ID AH014662; SV 2; linear; genomic DNA; STD; HUM; 1022 BP.
XX
AC AH014662; AY887665-AY887667;
XX
DT 31-JUL-2011 (Rel. 109, Created)
DT 31-JUL-2011 (Rel. 109, Last updated, Version 1)
XX
DE Homo sapiens MHC class I antigen (HLA-C) gene, HLA-Cw*010201 variant
DE allele, partial 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 1-1022
RA Oh H.B., Hur S.S., Lee M.N., Hong S.A., Kwon O.J.;
RT ;
RL Submitted (14-JAN-2005) to the INSDC.
RL Molecular Genetics, BioSewoom Institute of Bioscience & Biotechnology,
RL Wooyoung Technocenter 1F, #273-15, Sungsu 2-ga 3-dong, Sungdong-gu, Seoul
RL 133-831, Republic of Korea
XX
DR MD5; 1a40ebcc725d14ab77a142f5ccc2a7ee.
XX
CC On or before Jul 29, 2011 this sequence version replaced
CC gi:59665549, gi:59665550, gi:59665551, gi:59665548.
XX
FH Key Location/Qualifiers
FH
FT source 1..1022
FT /organism="Homo sapiens"
FT /chromosome="6"
FT /map="6p21.3"
FT /mol_type="genomic DNA"
FT /db_xref="taxon:9606"
FT gene <1..>1022
FT /gene="HLA-C"
FT /allele="HLA-Cw*010201 variant"
FT mRNA join(<1..270,371..646,747..>1022)
FT /gene="HLA-C"
FT /allele="HLA-Cw*010201 variant"
FT /product="MHC class I antigen"
FT CDS join(<1..270,371..646,747..>1022)
FT /codon_start=3
FT /gene="HLA-C"
FT /allele="HLA-Cw*010201 variant"
FT /product="MHC class I antigen"
FT /db_xref="InterPro:IPR001039"
FT /db_xref="InterPro:IPR003006"
FT /db_xref="InterPro:IPR003597"
FT /db_xref="InterPro:IPR007110"
FT /db_xref="InterPro:IPR011161"
FT /db_xref="InterPro:IPR011162"
FT /db_xref="InterPro:IPR013783"
FT /db_xref="UniProtKB/TrEMBL:Q5EFR2"
FT /protein_id="AAW88385.1"
FT /translation="SHSMKYFFTSVSRPGRGEPRFISVGYVDDTQFVRFDSDAASPRGE
FT PRAPWVEQEGPEYWDRETQKYKRQAQTDRVSLRNLRGYYNQSEAGSHTLQWMCGCDLGP
FT DGRLLRGYDQYAYDGKDYIALNEDLRSWTAADTAAQITQRKWEAAREAEQRRAYLEGTC
FT VEWLRRYLENGKETLQRAKHPKTHVTHHPVSDHEATLRCWALGFYPAEITLTWQWDGED
FT QTQDTELVETRPAGDGTFQKWAAVMVPSGEEQRYTCHVQHEGLPEPLTLRW"
FT exon 1..270
FT /gene="HLA-C"
FT /allele="HLA-Cw*010201 variant"
FT /number=2
FT gap 271..370
FT /estimated_length=unknown
FT exon 371..646
FT /gene="HLA-C"
FT /allele="HLA-Cw*010201 variant"
FT /number=3
FT gap 647..746
FT /estimated_length=unknown
FT exon 747..1022
FT /gene="HLA-C"
FT /allele="HLA-Cw*010201 variant"
FT /number=4
XX
SQ Sequence 1022 BP; 171 A; 251 C; 285 G; 115 T; 200 other;
gctcccactc catgaagtat ttcttcacat ccgtgtcccg gcctggccgc ggagagcccc 60
gcttcatctc agtgggctac gtggacgaca cgcagttcgt gcggttcgac agcgacgccg 120
cgagtccgag aggggagccg cgggcgccgt gggtggagca ggaggggccg gagtattggg 180
accgggagac acagaagtac aagcgccagg cacagactga ccgagtgagc ctgcggaacc 240
tgcgcggcta ctacaaccag agcgaggccg nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 300
nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 360
nnnnnnnnnn ggtctcacac cctccagtgg atgtgtggct gcgacctggg gcccgacggg 420
cgcctcctcc gcgggtatga ccagtacgcc tacgacggca aggattacat cgccctgaac 480
gaggacctgc gctcctggac cgccgcggac accgcggctc agatcaccca gcgcaagtgg 540
gaggcggccc gtgaggcgga gcagcggaga gcctacctgg agggcacgtg cgtggagtgg 600
ctccgcagat acctggagaa cgggaaggag acgctgcagc gcgcgannnn nnnnnnnnnn 660
nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 720
nnnnnnnnnn nnnnnnnnnn nnnnnnaaca cccaaagaca cacgtgaccc accatcccgt 780
ctctgaccat gaggccaccc tgaggtgctg ggccctgggc ttctaccctg cggagatcac 840
actgacctgg cagtgggatg gggaggacca aactcaggac accgagcttg tggagaccag 900
gccagcagga gatggaacct tccagaagtg ggcagctgtg atggtgcctt ctggagaaga 960
gcagagatac acgtgccatg tgcagcacga ggggctgccg gagcccctca ccctgagatg 1020
gg 1022
//
