ID KF413873; SV 1; linear; genomic DNA; STD; HUM; 1022 BP.
XX
AC KF413873;
XX
DT 11-NOV-2013 (Rel. 118, Created)
DT 11-NOV-2013 (Rel. 118, Last updated, Version 1)
XX
DE Homo sapiens MHC class I antigen (HLA) gene, HLA-A*02new allele, exons 2
DE through 4 and 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 Wang T.;
RT ;
RL Submitted (16-JUL-2013) to the INSDC.
RL HLA Lab, Xi`an Blood Center, 407 Zhuque Street, Xi`an, Shaanxi 710061,
RL China
XX
DR MD5; a6d70b8bea8286be0bd109078a2f3e3a.
DR IMGT/HLA; HLA-A*02:437; HLA09819.
XX
CC ##Assembly-Data-START##
CC Sequencing Technology :: Sanger dideoxy sequencing
CC ##Assembly-Data-END##
XX
FH Key Location/Qualifiers
FH
FT source 1..1022
FT /organism="Homo sapiens"
FT /mol_type="genomic DNA"
FT /db_xref="taxon:9606"
FT gene <1..>1022
FT /gene="HLA"
FT /allele="HLA-A*02new"
FT mRNA join(<1..270,371..646,747..>1022)
FT /gene="HLA"
FT /allele="HLA-A*02new"
FT /product="MHC class I antigen"
FT CDS join(<1..270,371..646,747..>1022)
FT /codon_start=3
FT /gene="HLA"
FT /allele="HLA-A*02new"
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="InterPro:IPR036179"
FT /db_xref="InterPro:IPR037055"
FT /db_xref="UniProtKB/TrEMBL:U5XMI1"
FT /protein_id="AGZ63888.1"
FT /translation="SHSMRYFFTSVSRPGRGEPRFIAVGYVDDTQFVRFDSDAASQRME
FT PRAPWIEQEGPEYWDGETRKVKAHSQTHRVDLGTLRGYYNQSEAGSHTVQRMCGCDVGS
FT DWRFLRGYHQYAYDGKDYIALKEDLRSWTAADMAAQTTKHKWEAAHVAEQLRAYLEGTC
FT VEWLRRYLENGKETLQRTDAPKTHMTHHAVSDHEATLRCWALSFYPAEITLTWQRDGED
FT QTQDTELVETRPAGDGTFQKWAAVVVPSGQEQRYTCHVQHEGLPKPLTLRW"
FT exon 1..270
FT /gene="HLA"
FT /allele="HLA-A*02new"
FT /number=2
FT gap 271..370
FT /estimated_length=unknown
FT exon 371..646
FT /gene="HLA"
FT /allele="HLA-A*02new"
FT /number=3
FT variation 586
FT /gene="HLA"
FT /replace="g"
FT variation 587
FT /gene="HLA"
FT /replace="a"
FT variation 590
FT /gene="HLA"
FT /replace="t"
FT gap 647..746
FT /estimated_length=unknown
FT exon 747..1022
FT /gene="HLA"
FT /allele="HLA-A*02new"
FT /number=4
XX
SQ Sequence 1022 BP; 170 A; 244 C; 283 G; 125 T; 200 other;
gctctcactc catgaggtat ttcttcacat ccgtgtcccg gcccggccgc ggggagcccc 60
gcttcatcgc agtgggctac gtggacgaca cgcagttcgt gcggttcgac agcgacgccg 120
cgagccagag gatggagccg cgggcgccgt ggatagagca ggagggtccg gagtattggg 180
acggggagac acggaaagtg aaggcccact cacagactca ccgagtggac ctggggaccc 240
tgcgcggcta ctacaaccag agcgaggccg nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 300
nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 360
nnnnnnnnnn gttctcacac cgtccagagg atgtgtggct gcgacgtggg gtcggactgg 420
cgcttcctcc gcgggtacca ccagtacgcc tacgacggca aggattacat cgccctgaaa 480
gaggacctgc gctcttggac cgcggcggac atggcagctc agaccaccaa gcacaagtgg 540
gaggcggccc atgtggcgga gcagttgaga gcctacctgg agggcacgtg cgtggagtgg 600
ctccgcagat acctggagaa cgggaaggag acgctgcagc gcacggnnnn nnnnnnnnnn 660
nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 720
nnnnnnnnnn nnnnnnnnnn nnnnnnacgc ccccaaaacg catatgactc accacgctgt 780
ctctgaccat gaagccaccc tgaggtgctg ggccctgagc ttctaccctg cggagatcac 840
actgacctgg cagcgggatg gggaggacca gacccaggac acggagctcg tggagaccag 900
gcctgcaggg gatggaacct tccagaagtg ggcggctgtg gtggtgcctt ctggacagga 960
gcagagatac acctgccatg tgcagcatga gggtttgccc aagcccctca ccctgagatg 1020
gg 1022
//