Dbfetch
ID MN016345; SV 1; linear; genomic DNA; STD; HUM; 2710 BP.
XX
AC MN016345;
XX
DT 27-FEB-2020 (Rel. 143, Created)
DT 27-FEB-2020 (Rel. 143, Last updated, Version 1)
XX
DE Homo sapiens clone B_112403_06849 MHC class I antigen (HLA-B) gene,
DE complete 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 1-2710
RA Cereb N., Yang S.Y.;
RT "HLA new alleles found by Histogenetics";
RL Unpublished.
XX
RN [2]
RP 1-2710
RA Cereb N., Yang S.Y.;
RT ;
RL Submitted (03-JUN-2019) to the INSDC.
RL Histogenetics, 300 Executive Blvd, Ossining, NY 10562, USA
XX
DR MD5; 5aa598f0f4d5ba9bf8ce82f968036287.
XX
FH Key Location/Qualifiers
FH
FT source 1..2710
FT /organism="Homo sapiens"
FT /mol_type="genomic DNA"
FT /clone="B_112403_06849"
FT /db_xref="taxon:9606"
FT gene 1..>2710
FT /gene="HLA-B"
FT mRNA join(1..109,238..507,753..1028,1601..1876,1970..2086,
FT 2528..2560,2667..>2710)
FT /gene="HLA-B"
FT /product="MHC class I antigen"
FT exon 1..109
FT /gene="HLA-B"
FT /number=1
FT 5'UTR 1..36
FT /gene="HLA-B"
FT CDS join(37..109,238..507,753..1028,1601..1876,1970..2086,
FT 2528..2560,2667..2710)
FT /codon_start=1
FT /gene="HLA-B"
FT /product="MHC class I antigen"
FT /protein_id="QDK63040.1"
FT /translation="MLVMAPRTVLLLLSAALALTETWAGSHSMRYFYTSVSRPGRGEPR
FT FISVGYVDDTQFVRFDSDAASPREEPRAPWIEQEGPEYWDRNTQICKTNTQTDRESLRN
FT LRGYYNQSEAGSHTLQSMYGCDVGPDGRLLRGHNQYAYDGKDYIALNEDLSSWTAADTA
FT AQITQRKWEAARVAEQLRTYLEGTCVEWLRRYLENGKETLQRADPPKTHVTHHPISDHE
FT ATLRCWALGFYPAEITLTWQRDGEDQTQDTELVETRPAGDRTFQKWAAVVVPSGEEQRY
FT TCHVQHEGLPKPLTLRWEPSSQSTVPIVGIVAGLAVLAVVVIGAVVAAVMCRRKSSGGK
FT GGSYSQAASSDSAQGSDVSLTA"
FT intron 110..237
FT /gene="HLA-B"
FT /number=1
FT exon 238..507
FT /gene="HLA-B"
FT /number=2
FT intron 508..752
FT /gene="HLA-B"
FT /number=2
FT exon 753..1028
FT /gene="HLA-B"
FT /number=3
FT intron 1029..1600
FT /gene="HLA-B"
FT /number=3
FT exon 1601..1876
FT /gene="HLA-B"
FT /number=4
FT intron 1877..1969
FT /gene="HLA-B"
FT /number=4
FT exon 1970..2086
FT /gene="HLA-B"
FT /number=5
FT intron 2087..2527
FT /gene="HLA-B"
FT /number=5
FT exon 2528..2560
FT /gene="HLA-B"
FT /number=6
FT intron 2561..2666
FT /gene="HLA-B"
FT /number=6
FT exon 2667..>2710
FT /gene="HLA-B"
FT /number=7
XX
SQ Sequence 2710 BP; 511 A; 812 C; 851 G; 536 T; 0 other;
cacccacccg gactcagagt ctcctcagac gccgagatgc tggtcatggc gccccgaacc 60
gtcctcctgc tgctctcggc ggccctggcc ctgaccgaga cctgggccgg tgagtgcggg 120
tcgggaggga aatggcctct gccgggagga gcgaggggac cgcaggcggg ggcgcaggac 180
ctgaggagcc gcgccgggag gagggtcggg cgggtctcag cccctcctcg cccccaggct 240
cccactccat gaggtatttc tacacctccg tgtcccggcc cggccgcggg gagccccgct 300
tcatctcagt gggctacgtg gacgacacgc agttcgtgag gttcgacagc gacgccgcga 360
gtccgagaga ggagccgcgg gcgccgtgga tagagcagga ggggccggaa tattgggacc 420
ggaacacaca gatctgcaag accaacacac agactgaccg agagagcctg cggaacctgc 480
gcggctacta caaccagagc gaggccggtg agtgaccccg gcccggggcg caggtcacga 540
ctccccatcc cccacgtacg gcccgggtcg ccccgagtct ccgggtccga gatccgcctc 600
cctgaggccg cgggacccgc ccagaccctc gaccggcgag agccccaggc gcgtttaccc 660
ggtttcattt tcagttgagg ccaaaatccc cgcgggttgg tcggggcggg gcggggctcg 720
ggggactggg ctgaccgcgg ggccggggcc agggtctcac accctccaga gcatgtacgg 780
ctgcgacgtg gggccggacg ggcgcctcct ccgcgggcat aaccagtacg cctacgacgg 840
caaggattac atcgccctga acgaggacct gagctcctgg accgcggcgg acaccgcggc 900
tcagatcacc cagcgcaagt gggaggcggc ccgtgtggcg gagcagctga gaacctacct 960
ggagggcacg tgcgtggagt ggctccgcag atacctggag aacgggaagg agacgctgca 1020
gcgcgcgggt accaggggca gtggggagcc ttccccatct cctataggtc gccggggatg 1080
gcctccaacg agaagaagag gaaaatggga tcagcgctag aatgtcgccc tcccttgaat 1140
ggagaatggc atgagttttc ctgagtttcc tctgagggcc ccctcttctc tctaggacaa 1200
ttaagggatg acgtctctga ggaaatggag gggaagacag tccctagaat actgatcagg 1260
ggtccccttt gacccctgca gcagccttgg gaaccatgac ttttcctctc aggccttgtt 1320
ctctgcctca cactcagtgt gtttggggct ctgattccag cacttctgag tcactttacc 1380
tccactcaga tcaggagcag aagtctctgt tccccgctca gagactcgaa ctttccaatg 1440
aatagattat cccaggtgcc tgcgtccagg ctggtgtctg ggttctgtgc cccttcccca 1500
ccccaggtgt cctgtccatt ctcaggctgg tcacatgggt ggtcctaggg tgtcccatga 1560
gagatgcaaa gcgcctgaat tttctgactc ttcccatcag accccccaaa gacacatgtg 1620
acccaccacc ccatctctga ccatgaggcc accctgaggt gctgggccct gggcttctac 1680
cctgcggaga tcacactgac ctggcagcgg gatggcgagg accaaactca ggacaccgag 1740
cttgtggaga ccagaccagc aggagacaga accttccaga agtgggcagc tgtggtggtg 1800
ccttctggag aagagcagag atacacatgc catgtacagc atgaggggct gccgaagccc 1860
ctcaccctga gatggggtaa ggagggggat gaggggtcat atctcttctc agggaaagca 1920
ggagcccttc agcagggtca gggcccctca tcttcccctc ctttcccaga gccatcttcc 1980
cagtccaccg tccccatcgt gggcattgtt gctggcctgg ctgtcctagc agttgtggtc 2040
atcggagctg tggtcgctgc tgtgatgtgt aggaggaaga gttcaggtag ggaaggggtg 2100
aggggtgggg tctgggtttt cttgtcccac tgggggtttc aagccccagg tagaagtgtt 2160
ccctgcatca ttactgggaa gcagcatgca cacaggggct aacgcagcct gggaccctgt 2220
gtgccagcac ttactctttt gtgcagcaca tgtgacaatg aaggacggat gtatcacctt 2280
gatggttgtg gtgttggggt cctgattcca gcattcatga gtcaggggaa ggtccctgct 2340
aaggacagac cttaggaggg cagttggtcc aggacccaca cttgctttcc tcgtgtttcc 2400
tgatcctgcc ctgggtctgt agtcatactt ctggaaattc cttttgggtc caagactagg 2460
aggttcctct aagatctcat ggccctgctt cctcccagtc ccctcacagg acattttctt 2520
cccacaggtg gaaaaggagg gagctactct caggctgcgt gtaagtggtg ggggtgggag 2580
tgtggaggag ctcacccacc ccataattcc tcctgtccca cgtctcctgt gggctctgac 2640
caggtcctgt ttttgttcta ctccagccag cgacagtgcc cagggctctg atgtgtctct 2700
cacagcttga 2710
//