Dbfetch

ID   ON110786; SV 1; linear; genomic DNA; STD; HUM; 3353 BP.
XX
AC   ON110786;
XX
DT   31-MAY-2023 (Rel. 144, Created)
DT   01-JUN-2023 (Rel. 144, Last updated, Version 1)
XX
DE   Homo sapiens MHC class I antigen (HLA-C) gene, HLA-C*07var allele, complete
DE   cds.
XX
KW   .
XX
OS   Homo sapiens (human)
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Homo.
XX
RN   [1]
RP   1-3353
RA   Bola R.K., De Mendonca E.;
RT   ;
RL   Submitted (28-MAR-2022) to the INSDC.
RL   Scientific Development, Anthony Nolan Histocompatibility Laboratory, 77B
RL   Fleet Road, London NW3 2QU, United Kingdom
XX
DR   MD5; ab6bf701e6ba104dfb9add8b9e1f5d86.
XX
CC   ##Assembly-Data-START##
CC   Assembly Method       :: NGSengine v. 2.25
CC   Sequencing Technology :: Illumina
CC   ##Assembly-Data-END##
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..3353
FT                   /organism="Homo sapiens"
FT                   /mol_type="genomic DNA"
FT                   /db_xref="taxon:9606"
FT   gene            1..3353
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT   mRNA            join(1..364,495..764,1015..1290,1878..2153,2278..2397,
FT                   2836..2868,2976..3023,3188..3353)
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /product="MHC class I antigen"
FT   exon            1..364
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /number=1
FT   5'UTR           1..291
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT   CDS             join(292..364,495..764,1015..1290,1878..2153,2278..2397,
FT                   2836..2868,2976..3023,3188..3192)
FT                   /codon_start=1
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /product="MHC class I antigen"
FT                   /protein_id="UQZ09697.1"
FT                   /translation="MRVMAPRALLLLLSGGLALTETWACSHSMRYFDTAVSRPGRGEPR
FT                   FISVGYVDDTQFVRFDSDAASPRGEPRAPWVEQEGPEYWDRETQNYKRQAQADRVSLRN
FT                   LRGYYNQSEDGSHTLQRMYGCDLGPDGRLLRGYDQSAYDGKDYIALNEDLRSWTAADTA
FT                   AQITQRKLEAARAAEQLRAYLEGTCVEWLRRYLENGKETLQRAEPPKTHVTHHPLSDHE
FT                   ATLRCWALGFYPAEITLTWQRDGEDQTQDTELVETRPAGDGTFQKWAAVVVPSGQEQRY
FT                   TCHMQHEGLQEPLTLSWEPSSQPTIPIMGIVAGLAVLVVLAVLGAVVTAMMCRRKSSGG
FT                   KGGSCSQAACSNSAQGSDESLITCKA"
FT   intron          365..494
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /number=1
FT   exon            495..764
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /number=2
FT   intron          765..1014
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /number=2
FT   exon            1015..1290
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /number=3
FT   intron          1291..1877
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /number=3
FT   exon            1878..2153
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /number=4
FT   intron          2154..2277
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /number=4
FT   exon            2278..2397
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /number=5
FT   intron          2398..2835
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /number=5
FT   exon            2836..2868
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /number=6
FT   intron          2869..2975
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /number=6
FT   exon            2976..3023
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /number=7
FT   intron          3024..3187
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /number=7
FT   exon            3188..3353
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
FT                   /number=8
FT   3'UTR           3193..3353
FT                   /gene="HLA-C"
FT                   /allele="HLA-C*07var"
XX
SQ   Sequence 3353 BP; 623 A; 987 C; 1046 G; 697 T; 0 other;
     aggagaagag ggatcaggac gaagtcccag gtcccggacg gggctctcag ggtctcaggc        60
     tccaagggcc gtgtctgcat tggggaggcg ccgcgttggg gattctccac tcccctgagt       120
     ttcacttctc ccaacctgcg tcgggtcctt cttcctgaat actcatgacg cgtccccaat       180
     tcccactccc attgggtgtc gggttctaga gaagccaatc agcgtctccg cagtcccggt       240
     tctaaagtcc ccagtcaccc acccggactc acattctccc cagaggccga gatgcgggtc       300
     atggcgcccc gagccctcct cctgctgctc tcgggaggcc tggccctgac cgagacctgg       360
     gcctgtgagt gcggggttgg gagggaagcg gcctctgcgg agaggagcga ggggcccgcc       420
     cggcgagggc gcaggacccg gggagccgcg cagggaggtg ggtcgggcgg gtctcagccc       480
     ctcctcgccc ccaggctccc actccatgag gtatttcgac accgccgtgt cccggcccgg       540
     ccgcggagag ccccgcttca tctcagtggg ctacgtggac gacacgcagt tcgtgcggtt       600
     cgacagcgac gccgcgagtc cgagagggga gccgcgggcg ccgtgggtgg agcaggaggg       660
     gccggagtat tgggaccggg agacacagaa ctacaagcgc caggcacagg ctgaccgagt       720
     gagcctgcgg aacctgcgcg gctactacaa ccagagcgag gacggtgagt gaccccggcc       780
     cggggcgcag gtcacgaccc ctccccatcc cccacggacg gcccgggtcg ccccgagtct       840
     ccccgtctga gatccacccc aaggtggatc tgcggaaccc gcccagaccc tcgaccggag       900
     agagccccag tcgcctttac ccggtttcat tttcggttta ggccaaaatc cccgcgggtt       960
     ggtcggggcg gggcggggct cgggggactg ggctgaccgc gggggcgggg ccagggtctc      1020
     acaccctcca gaggatgtat ggctgcgacc tggggcccga cgggcgcctc ctccgcgggt      1080
     atgaccagtc cgcctacgac ggcaaggatt acatcgccct gaacgaggac ctgcgctcct      1140
     ggaccgccgc ggacaccgcg gctcagatca cccagcgcaa gttggaggcg gcccgtgcgg      1200
     cggagcagct gagagcctac ctggagggca cgtgcgtgga gtggctccgc agatacctgg      1260
     agaacgggaa ggagacgctg cagcgcgcgg gtaccagggg cagtggggag ccttccccat      1320
     ctcctataga tctcccggga tggcctccca cgaggagggg aggaaaatgg gatcagcact      1380
     ggaatatcgc cctcccttga atggagaatg gcatgagttt tcctgagttt cctctgaggg      1440
     ccccctctgc tctctaggac aattaaggga tgaagtctct gaggaaatgg aggggaagac      1500
     agtccctgga atactgatca ggggtctcct ttgaccactt tgaccactgc agcagctgtg      1560
     gtcaggctgc tgacctttct ctcaggcctt gttctctgcc tcacactcaa tgtgtctgaa      1620
     ggtttgattc cagcttttct gagtcctgca gcctccactc aggtcaggac cagaagtcgc      1680
     tgttcctccc tcagagacta gaactttcca atgaatagga gattatccca ggtgcctgtg      1740
     tccaggctgg cgtctgggtt ctgtgccgcc ttccccaccc caggtgtcct gtccattctc      1800
     aggatggtca catgggcgct gctggagtgt cccaagagag atgcaaagtg tctgaatttt      1860
     ctgactcttc ccgtcagaac ccccaaagac acacgtgacc caccaccccc tctctgacca      1920
     tgaggccacc ctgaggtgct gggccctggg cttctaccct gcggagatca cactgacctg      1980
     gcagcgggat ggggaggacc agacccagga caccgagctt gtggagacca ggccagcagg      2040
     agatggaacc ttccagaagt gggcagctgt ggtggtgcct tctggacaag agcagagata      2100
     cacgtgccat atgcagcacg aggggctgca agagcccctc accctgagct ggggtaagga      2160
     ggggaatggg gggtcacatc tcttatcaga gaaagcagaa gtccttctgg agcccttcag      2220
     ccgggtcagg gctgaggctt gggggtcagg gcccctcacc ttctcctcct ttcccagagc      2280
     catcttccca gcctaccatc cccatcatgg gcatcgttgc tggcctggct gtcctggttg      2340
     tcctagctgt ccttggagct gtggtcaccg ctatgatgtg taggaggaag agctcaggta      2400
     gggaaggggt gaagagcggg gtctgggttt tcttgtccca ctgggagttt caagccccag      2460
     gtagaagtgt gccccgcctt gttactggaa gcaccatcca cacatgggcc atcccagcct      2520
     gggaccctgt gtgccagcac ttactctttt gtgacacatg tgacaatgaa ggacggatgt      2580
     atcaccttga tgattatggt gttggggtcc tgattccagc attcatgagt caggggaagg      2640
     tccctgctaa ggacagacct taggagggca gttggtccag aacccacaac tgctttcccc      2700
     atgtttcctg atcctgccct gggtctgcag tcgtagttct ggaaacttct cttgggtcca      2760
     agactaggag gttcccctaa gatcacatgg ccctgcctcc tcccagtccc ctcatagggc      2820
     attttcttcc cacaggtgga aaaggaggga gctgctctca ggctgcgtgt aagtgatggc      2880
     ggcgggcgtg tggaggagct cacctactcc ataattcctc ttgtcccaca tctcctgcgg      2940
     gctctgacca ggtctttttt tttgttctac cccaggcagc aacagtgccc agggctctga      3000
     tgagtctctc atcacttgta aaggtgagat tctggggagc tgaagtggtc gggggtgggg      3060
     cagagggaaa aggcctgggt aatggggatt ctttgattgg gacgtttcga gtgtgtggtg      3120
     ggccgttcag agtgtcatca cttaccatga ctgacctgaa tttgttcatg actattgtgt      3180
     tctgtagcct gagacagctg cctgtgtggg actgagatgc aggatttctt cacacctctc      3240
     ctttgtgact tcaagagcct ctggcatctc tttctgcaaa ggcgtctgaa tgtgtctgcg      3300
     ttcctgttag cataatgtga ggaggtggag agacagccca cccccgtgtc cac             3353
//