Dbfetch
ID MN016506; SV 1; linear; genomic DNA; STD; HUM; 2710 BP.
XX
AC MN016506;
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_07010 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RL Unpublished.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; cdf0d16ba4b78ee9af7ee0e3fc6c878b.
XX
FH Key Location/Qualifiers
FH
FT source 1..2710
FT /organism="Homo sapiens"
FT /mol_type="genomic DNA"
FT /clone="B_112403_07010"
FT /db_xref="taxon:9606"
FT gene 1..>2710
FT /gene="HLA-B"
FT mRNA join(1..109,238..507,754..1029,1602..1877,1971..2087,
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..507,754..1029,1602..1877,1971..2087,
FT 2528..2560,2667..2710)
FT /codon_start=1
FT /gene="HLA-B"
FT /product="MHC class I antigen"
FT /protein_id="QDK63201.1"
FT /translation="MLVMAPRTVLLLLSAALALTETWAGSHSMRYFYTAVSRPGRGEPR
FT FISVGYVDDTQFVRFDSDAASPREEPRAPWIEQEGPEYWDRNTQICKTNTQTDRESLRN
FT LRGYYNQSEAGSHTLQWMYGCDVGPDGRLLRGYNQFAYDGKDYIALNEDLSSWTAADTA
FT AQITQRKWEAAREAEQLRAYLEGTCVEWLRRHLENGKETLQRADPPKTHVTHHPISDHE
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..753
FT /gene="HLA-B"
FT /number=2
FT exon 754..1029
FT /gene="HLA-B"
FT /number=3
FT intron 1030..1601
FT /gene="HLA-B"
FT /number=3
FT exon 1602..1877
FT /gene="HLA-B"
FT /number=4
FT intron 1878..1970
FT /gene="HLA-B"
FT /number=4
FT exon 1971..2087
FT /gene="HLA-B"
FT /number=5
FT intron 2088..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; 509 A; 806 C; 857 G; 538 T; 0 other;
cacccacccg gactcagagt ctcctcagac gccaagatgc tggtcatggc gccccgaacc 60
gtcctcctgc tgctctcggc ggccctggcc ctgaccgaga cctgggccgg tgagtgcggg 120
tcgggaggga aatggcctct gccgggagga gcgaggggac cgcaggcggg ggcgcaggac 180
ctgaggagcc gcgccgggag gagggtcggg cgggtttcag cccctcctcg cccccaggct 240
cccactccat gaggtatttc tacaccgccg 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 cccacggacg gcccgggtcg ccccgagtct ccgggtccga gatccgcctc 600
cctgaggccg cgggacccgc ccagaccctc gaccggcgag agccccaggc gcgtttaccc 660
ggtttcattt tcagttgagg ccaaaatccc cgcgggttgg gcggggcggg gcggggctcg 720
gggggactgg gctgaccgcg ggggcggggc cagggtctca caccctccag tggatgtatg 780
gctgcgacgt ggggccggac gggcgcctcc tccgcgggta taaccagttc gcctacgacg 840
gcaaggatta catcgccctg aacgaggacc tgagctcctg gaccgcggcg gacaccgcgg 900
ctcagatcac ccagcgcaag tgggaggcgg cccgtgaggc ggagcagctg agagcctacc 960
tggagggcac gtgcgtggag tggctccgca gacacctgga gaacgggaag gagacgctgc 1020
agcgcgcggg taccaggggc agtggggagc cttccccatc tcctataggt cgccggggat 1080
ggcctcccac gagaagaaga ggaaaatggg atcagcgcta gaatgtcgcc ctcccttgaa 1140
tggagaatgg catgagtttt cctgagtttc ctctgagggc cccctcttct ctctaggaca 1200
attaagggat gacgtctctg aggaaatgga ggggaagaca gtccctagaa tactgatcag 1260
gggtcccctt tgacccctgc agcagccttg ggaaccatga cttttcttct caggccttgt 1320
tctctgcctc acactcagtg tgtttggggc tctgattcca gcacttctga gtcactttac 1380
ctccactcag atcaggagca gaagtctctg ttccccgctc agagactcga actttccaat 1440
gaatagatta tcccaggtgc ctgcgtccag gctggtgtct gggttctgtg tcccttcccc 1500
accccaggtg tcctgtccat tctcaggctg gtcacatggg tggtcctagg gtgtcccatg 1560
agagatgcaa agcgcctgaa ttttctgact cttcccatca gaccccccaa agacacatgt 1620
gacccaccac cccatctctg accatgaggc caccctgagg tgctgggccc tgggcttcta 1680
ccctgcggag atcacactga cctggcagcg ggatggcgag gaccaaactc aggacaccga 1740
gcttgtggag accagaccag caggagacag aaccttccag aagtgggcag ctgtggtggt 1800
gccttctgga gaagagcaga gatacacatg ccatgtacag catgaggggc tgccgaagcc 1860
cctcaccctg agatggggta aggaggggga tgaggggtca tatctcttct cagggaaagc 1920
aggagccctt cagcagggtc agggcccctc atcttcccct cctttcccag agccatcttc 1980
ccagtccacc gtccccatcg tgggcattgt tgctggcctg gctgtcctag cagttgtggt 2040
catcggagct gtggtcgctg ctgtgatgtg taggaggaag agttcaggta gggaaggggt 2100
gaggggtggg gtctgggttt tcttgtccca ctgggggttt caagccccag gtagaagtgt 2160
tcctgcatca 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
//