Dbfetch
ID MN994975; SV 1; linear; genomic DNA; STD; HUM; 2967 BP.
XX
AC MN994975;
XX
DT 10-MAR-2021 (Rel. 144, Created)
DT 10-MAR-2021 (Rel. 144, Last updated, Version 1)
XX
DE Homo sapiens clone C_112638_08647 MHC class I antigen (HLA-C) 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 1-2967
RA Cereb N., Yang S.Y.;
RT "HLA new alleles found by Histogenetics";
RL Unpublished.
XX
RN [2]
RP 1-2967
RA Cereb N., Yang S.Y.;
RT ;
RL Submitted (27-JAN-2020) to the INSDC.
RL Histogenetics, 300 Executive Blvd, Ossining, NY 10562, USA
XX
DR MD5; 1931c3c6434e40d25a2b43755502f122.
XX
FH Key Location/Qualifiers
FH
FT source 1..2967
FT /organism="Homo sapiens"
FT /mol_type="genomic DNA"
FT /clone="C_112638_08647"
FT /db_xref="taxon:9606"
FT gene 1..2967
FT /gene="HLA-C"
FT mRNA join(1..137,268..537,784..1059,1647..1922,2044..2163,
FT 2603..2635,2743..2790,2955..2967)
FT /gene="HLA-C"
FT /product="MHC class I antigen"
FT exon 1..137
FT /gene="HLA-C"
FT /number=1
FT 5'UTR 1..64
FT /gene="HLA-C"
FT CDS join(65..137,268..537,784..1059,1647..1922,2044..2163,
FT 2603..2635,2743..2790,2955..2959)
FT /codon_start=1
FT /gene="HLA-C"
FT /product="MHC class I antigen"
FT /protein_id="QIA49066.1"
FT /translation="MRVMAPRTLILLLSGALALTETWACSHSMRYFSTSVSRPGRGEPR
FT FIAVGYVDDTQFVRFDSDAASPRGEPRAPWVEQEGPEYWDRETQKYKRQAQTDRVSLRN
FT LRGYYNQSEAGSHTLQWMFGCDLGPDGRLLRGYDQSAYDGKDYIALNEDLRSWTAADTA
FT AQITQRKWEAAREAEQRRAYLEGTCMEWLRRYLENGKETLQRAEHPKTHVTHHPVSDHE
FT ATLRCWALGFYPAEITLTWQWDGEDQTQDTELVETRPAGDGTFQKWAAVVVPSGEEQRY
FT TCHVQHEGLPEPLTLRWEPSSQPTIPIVGIVAGLAVLAVLAVLGAVVAVVMCRRKSSGG
FT KGGSCSQAASSNSAQGSDESLIACKA"
FT intron 138..267
FT /gene="HLA-C"
FT /number=1
FT exon 268..537
FT /gene="HLA-C"
FT /number=2
FT intron 538..783
FT /gene="HLA-C"
FT /number=2
FT exon 784..1059
FT /gene="HLA-C"
FT /number=3
FT intron 1060..1646
FT /gene="HLA-C"
FT /number=3
FT exon 1647..1922
FT /gene="HLA-C"
FT /number=4
FT intron 1923..2043
FT /gene="HLA-C"
FT /number=4
FT exon 2044..2163
FT /gene="HLA-C"
FT /number=5
FT intron 2164..2602
FT /gene="HLA-C"
FT /number=5
FT exon 2603..2635
FT /gene="HLA-C"
FT /number=6
FT intron 2636..2742
FT /gene="HLA-C"
FT /number=6
FT exon 2743..2790
FT /gene="HLA-C"
FT /number=7
FT intron 2791..2954
FT /gene="HLA-C"
FT /number=7
FT exon 2955..2967
FT /gene="HLA-C"
FT /number=8
FT 3'UTR 2960..2967
FT /gene="HLA-C"
XX
SQ Sequence 2967 BP; 553 A; 863 C; 947 G; 604 T; 0 other;
ccgcagtccc ggttctaaag tccccagtca cccacccgga ctcagattct ccccagacgc 60
cgagatgcgg gtcatggcgc cccgaaccct catcctgctg ctctcgggag ccctggccct 120
gaccgagacc tgggcctgtg agtgcggggt taggagggaa acggcctctg cggagaggag 180
cgaggggccc gcccggcgag ggcgcaggac ccggggagcc gcgcagggag gagggtcggg 240
cgggtctcag ccactcctcg tccccaggct cccactccat gaggtatttc tccacatccg 300
tgtcccggcc cggccgcggg gagccccgct tcatcgcagt gggctacgtg gacgacacgc 360
agttcgtgcg gttcgacagc gacgccgcga gtccgagagg ggagccgcgg gcgccgtggg 420
tggagcagga ggggccggag tattgggacc gggagacaca gaagtacaag cgccaggcac 480
agactgaccg agtgagcctg cggaacctgc gcggctacta caaccagagc gaggccggtg 540
agtgaccccg gcccggggcg caggtcacga cccctcccca tcccccacgg acggcccggg 600
tcgccccgag tctccccgtc tgagatccac cccgaggctg cggaacccgc ccagaccctc 660
gaccggagag agccccagtc acctttaccc ggtttcattt tcagtttagg ccaaaatccc 720
cgcgggttgg tcgggactgg ggcggggctc gggggacggg gctgaccacg ggggcggggc 780
cagggtctca caccctccag tggatgtttg gctgcgacct ggggcccgac gggcgcctcc 840
tccgcgggta tgaccagtcc gcctacgacg gcaaggatta catcgccctg aacgaggatc 900
tgcgctcctg gaccgccgcg gacacggcgg ctcagatcac ccagcgcaag tgggaggcgg 960
cccgtgaggc ggagcagcgg agagcctacc tggagggcac gtgcatggag tggctccgca 1020
gatacctgga gaacgggaag gagacgctgc agcgcgcggg taccaggggc agtggggagc 1080
cttccccatc tcccgtagat ctcccgggat ggcctcccac gaggagggga ggaaaatggg 1140
atcagcgcta gaatatcgcc ctcccttgaa tggagaatgg gatgagtttt cctgagtttc 1200
ctctgagggc cccctctgct ctctaggaca attaagggat gaagtccttg aggaaatgga 1260
ggggaagaca gtccctggaa tactgatcag gggtcccctt tgaccacttt gaccactgca 1320
gcagctgtgg tcaggctgct gacctttctc tcaggccttg ttctctgcct cacgctcaat 1380
gtgtttgaag gtttgattcc agcttttctg agtccttcgg cctccactca ggtcaggacc 1440
agaagtcgct gttcctccct cagagactag aactttccaa tgaataggag attatcccag 1500
gtgcctgtgt ccaggctggc gtctgggttc tgtgccccct tccccacccc aggtgtcctg 1560
tccattctca ggatggtcac atgggcgctg ttggagtgtc gcaagagaga tacaaagtgt 1620
ctgaattttc tgactcttcc cgtcagaaca cccaaagaca cacgtgaccc accatcccgt 1680
ctctgaccat gaggccaccc tgaggtgctg ggccctgggc ttctaccctg cggagatcac 1740
actgacctgg cagtgggatg gggaggacca aactcaggac accgagcttg tggagaccag 1800
gccagcagga gatggaacct tccagaagtg ggcagctgtg gtggtgcctt ctggagaaga 1860
gcagagatac acgtgccatg tgcagcacga ggggctgccg gagcccctca ccctgagatg 1920
gggtaaggag ggggatgagg ggtgatgtgt cttctcaggg aaagcagaag tcctggagcc 1980
cttcagccgg gtcagggctg aggcttggag gtcagggccc ctcaccttcc cctcctttcc 2040
cagagccgtc ttcccagccc accatcccca tcgtgggcat cgttgctggc ctggctgtcc 2100
tggctgtcct agctgtccta ggagctgtgg tggctgttgt gatgtgtagg aggaagagct 2160
caggtaggga aggggtgagg agtggggtct gggttttctt gttccactgg gagtttcaag 2220
ccccaggtag aagtgtgccc cacctcgtta ctggaagcac catccacaca tgggccatcc 2280
cagcctggga ccctgtgtgc cagcacttac tctgttgtga agcacatgac aatgaaggac 2340
agatgtatca ccttgatgat tatggtgttg gggtccttga ttccagcatt catgagtcag 2400
gggaaggtcc ctgctaagga cagaccttag gagggcagtt gcttcaggac ccacagctgc 2460
tttccccgtg tttcctgatc ctgccctggg tctgcagtca tagttctgga aacttctctt 2520
gggtccaaga ctaggaggtt cccctaagat cgcatggccc tgcctcctcc ctgtcccctc 2580
acagggcatt ttcttcccac aggtggaaaa ggagggagct gctctcaggc tgcgtgtaag 2640
tgatggcggt gggcgtgtgg aggagctcac ccaccccata attcctcttg tcccacatct 2700
cctgcgggct ctgaccaggt cttttttttt gttctacccc agccagcaac agtgcccagg 2760
gctctgatga gtctctcatc gcttgtaaag gtgagattct ggggagctga agtggtcggg 2820
ggtggggcag agggaaaagg cctgggtaat ggggatcctt tgattgggac gtttcgaatg 2880
tgtggtgagc tgttcagagt gtcatcactt accatgactg acctgaattt gttcatgact 2940
attgtgttct gtagcctgag acagctg 2967
//