Dbfetch

ID   MH325441; SV 1; linear; genomic DNA; STD; HUM; 2981 BP.
XX
AC   MH325441;
XX
DT   12-JUN-2018 (Rel. 137, Created)
DT   06-JUL-2018 (Rel. 137, Last updated, Version 2)
XX
DE   Homo sapiens MHC class I protein (HLA-B) gene, HLA-B*40var 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   1-2981
RA   Parab S., Sharma A., Pitale P., Morjaria M., Dedhia L., Khattry N.,
RA   Parekh S.;
RT   ;
RL   Submitted (04-MAY-2018) to the INSDC.
RL   HLA Lab, Marrow Donor Registry India, SL Raheja Hospital, 2nd Floor old
RL   Wing, Mahim, Mumbai, Maharashtra 400016, India
XX
DR   MD5; c9634beb0784f5799ffe4297b48d1182.
XX
CC   ##Assembly-Data-START##
CC   Assembly Method       :: Long Amplicon Analysis v. 5.1.0.26411
CC   Sequencing Technology :: Pacific Biosciences
CC   ##Assembly-Data-END##
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..2981
FT                   /organism="Homo sapiens"
FT                   /mol_type="genomic DNA"
FT                   /db_xref="taxon:9606"
FT   gene            <1..>2981
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT   mRNA            join(<1..348,477..746,992..1267,1842..2117,2211..2327,
FT                   2769..2801,2908..>2981)
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT                   /product="MHC class I protein"
FT   exon            <1..348
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT                   /number=1
FT   5'UTR           <1..275
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT   CDS             join(276..348,477..746,992..1267,1842..2117,2211..2327,
FT                   2769..2801,2908..2951)
FT                   /codon_start=1
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT                   /product="MHC class I protein"
FT                   /db_xref="GOA:A0A2U9AEP5"
FT                   /db_xref="InterPro:IPR001039"
FT                   /db_xref="InterPro:IPR003006"
FT                   /db_xref="InterPro:IPR003597"
FT                   /db_xref="InterPro:IPR007110"
FT                   /db_xref="InterPro:IPR010579"
FT                   /db_xref="InterPro:IPR011161"
FT                   /db_xref="InterPro:IPR011162"
FT                   /db_xref="InterPro:IPR013783"
FT                   /db_xref="InterPro:IPR036179"
FT                   /db_xref="InterPro:IPR037055"
FT                   /db_xref="UniProtKB/TrEMBL:A0A2U9AEP5"
FT                   /protein_id="AWO72996.1"
FT                   /translation="MRVTAPRTVLLLLSAALALTETWAGSHSMRYFHTAMSRPGRGEPR
FT                   FITVGYVDDTLFVRFDSDATSPRKEPRAPWIEQEGPEYWDRETQISKTNTQTYRESLRN
FT                   LRGYYNQSEAGSHTLQRMYGCDVGPDGRLLRGHNQYAYDGKDYIALNEDLRSWTAADTA
FT                   AQISQRKLEAAREAEQLRAYLEGECVEWLRRYLENGKDKLERADPPKTHVTHHPISDHE
FT                   ATLRCWALGFYPAEITLTWQRDGEDQTQDTELVETRPAGDRTFQKWAAVVVPSGEEQRY
FT                   TCHVQHEGLPKPLTLRWEPSSQSTVPIVGIVAGLAVLAVVVIGAVVAAVMCRRKSSGGK
FT                   GGSYSQAACSDSAQGSDVSLTA"
FT   intron          349..476
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT                   /number=1
FT   exon            477..746
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT                   /number=2
FT   intron          747..991
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT                   /number=2
FT   exon            992..1267
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT                   /number=3
FT   intron          1268..1841
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT                   /number=3
FT   exon            1842..2117
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT                   /number=4
FT   intron          2118..2210
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT                   /number=4
FT   exon            2211..2327
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT                   /number=5
FT   intron          2328..2768
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT                   /number=5
FT   exon            2769..2801
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT                   /number=6
FT   intron          2802..2907
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT                   /number=6
FT   exon            2908..>2981
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
FT                   /number=7
FT   3'UTR           2952..>2981
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40var"
XX
SQ   Sequence 2981 BP; 554 A; 893 C; 937 G; 597 T; 0 other;
     gaagtcccag gccccgggcg gggctctcag ggtctcaggc tccgagggcc gcgtctgcaa        60
     tggggaggcg cagcgttggg gattccccac tcccacgagt ttcacttctt ctcccaacct       120
     atgtcgggtc cttcttccag gatactcgtg acgcgtcccc atttcccact cccattgggt       180
     gtcgggtgtc tagagaagcc aatcagcgtc gccgtggtcc cagttctaaa gtccccacgc       240
     acccacccgg actcagaatc tcctcagacg ccgagatgcg ggtcacggca ccccgaaccg       300
     tcctcctgct gctctcggcg gccctggccc tgaccgagac ctgggccggt gagtgcgggt       360
     cggcagggaa atggcctctg tggggaggag cgaggggacc gcaggcgggg gcgcaggacc       420
     cggggagccg cgccgggagg agggtcgggc gggtctcagc tcctcctcgc ccccaggctc       480
     ccactccatg aggtatttcc acaccgccat gtcccggccc ggccgcgggg agccccgctt       540
     catcaccgtg ggctacgtgg acgacacgct gttcgtgagg ttcgacagcg acgccacgag       600
     tccgaggaag gagccgcggg cgccatggat agagcaggag gggccggagt attgggaccg       660
     ggagacacag atctccaaga ccaacacaca gacttaccga gagagcctgc ggaacctgcg       720
     cggctactac aaccagagcg aggccggtga gtgaccccgg cccggggcgc aggtcacgac       780
     tccccatccc ccacgtacgg cccgggtcgc cccgagtctc cgggtccgag atccgacccc       840
     ctgaggccgc gggacccgcc cagaccctcg accggcgaga gccccaggcg cgtttacccg       900
     gtttcatttt cagttgaggc caaaatcccc gcgggttggt cggggcgggg cggggctcgg       960
     gggactgggc tgaccgcggg gccggggcca gggtctcaca ccctccagag gatgtacggc      1020
     tgcgacgtgg ggccggacgg gcgcctcctc cgcgggcata accagtacgc ctacgacggc      1080
     aaggattaca tcgccctgaa cgaggacctg cgctcctgga ccgccgcgga cacggcggct      1140
     cagatctccc agcgcaagtt ggaggcggcc cgtgaggcgg agcagctgag agcctacctg      1200
     gagggcgagt gcgtggagtg gctccgcaga tacctggaga acgggaagga caagctggag      1260
     cgcgctggta ccaggggcag tggggagcct tccccatctc ctataggtcg ccggggatgg      1320
     cctcccacga gaagaggagg aaaatgggat cagcgctaga atgtcgccct ccgttgaatg      1380
     gagaatggca tgagttttcc tgagtttcct ctgagggccc cctcttctct ctagacaatt      1440
     aaggaatgac gtctctgagg aaatggaggg gaagacagtc cctagaatac tgatcagggg      1500
     tcccctttga cccctgcagc agccttggga accgtgactt ttcctctcag gccttgttct      1560
     ctgcctcaca ctcagtgtgt ttggggctct gattccagca cttctgagtc actttacctc      1620
     cactcagatc aggagcagaa gtccctgttc cccgctcaga gactcgaact ttccaatgaa      1680
     taggagatta tcccaggtgc ctgcgtccag gctggtgtct gggttctgtg ccccttcccc      1740
     accccaggtg tcctgtccat tctcaggctg gtcacatggg tggtcctagg gtgtcccatg      1800
     aaagatgcaa agcgcctgaa ttttctgact cttcccatca gaccccccaa agacacacgt      1860
     gacccaccac cccatctctg accatgaggc caccctgagg tgctgggccc tgggtttcta      1920
     ccctgcggag atcacactga cctggcagcg ggatggcgag gaccaaactc aggacactga      1980
     gcttgtggag accagaccag caggagatag aaccttccag aagtgggcag ctgtggtggt      2040
     gccttctgga gaagagcaga gatacacatg ccatgtacag catgaggggc tgccgaagcc      2100
     cctcaccctg agatggggta aggaggggga tgaggggtca tatctcttct cagggaaagc      2160
     aggagccctt cagcagggtc agggcccctc atcttcccct cctttcccag agccgtcttc      2220
     ccagtccacc gtccccatcg tgggcattgt tgctggcctg gctgtcctag cagttgtggt      2280
     catcggagct gtggtcgctg ctgtgatgtg taggaggaag agttcaggta gggaaggggt      2340
     gaggggtggg gtctgggttt tcttgtccca ctgggggttt caagccccag gtagaagtgt      2400
     tccctgcctc attactggga agcagcatgc acacaggggc taacgcagcc tgggaccctg      2460
     tgtgccagca cttactcttt tgtgcagcac atgtgacaat gaaggatgga tgtatcacct      2520
     tgatggttgt ggtgttgggg tcctgattcc agcattcatg agtcagggga aggtccctgc      2580
     taaggacaga ccttaggagg gcagttggtc caggacccac acttgctttc ctcgtgtttc      2640
     ctgatcctgc cctgggtctg tagtcatact tctggaaatt ccttttgggt ccaagactag      2700
     gaggttcctc taagatctca tggccctgct tcctcccagt gccctcacag gacattttct      2760
     tcccacaggt ggaaaaggag ggagctactc tcaggctgcg tgtaagtggt gggggtggga      2820
     gtgtggagga gctcacccac cccataattc ctcctgtccc acgtctcctg cgggctctga      2880
     ccaggtcctg tttttgttct actccaggca gcgacagtgc ccagggctct gatgtgtctc      2940
     tcacagcttg aaaaggtgag attcttgggg tctagagtgg g                          2981
//