Canonical Allele Identifier: CA2770463969
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944616_29944617dup , CM000668.2:g.29944616_29944617dup GRCh38
NC_000006.11:g.29912393_29912394dup , CM000668.1:g.29912393_29912394dup GRCh37
NC_000006.10:g.30020372_30020373dup NCBI36
NG_029217.2:g.7152_7153dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.895+219_895+220dup ENSP00000492789.2:n.895+219_895+220dup
ENST00000706892.1:n.1968_1969dup
ENST00000706893.1:c.1046_1047dup ENSP00000516609.1:p.Trp350GlyfsTer?
ENST00000706894.1:c.1012_1012+1dup
ENST00000706895.1:n.1390_1391dup
ENST00000706896.1:n.1866_1867dup
ENST00000706897.1:n.1288_1289dup
ENST00000706898.1:c.1012_1013dup ENSP00000516611.1:p.Gly339ValfsTer5
ENST00000706899.1:n.1866_1866+1dup
ENST00000706900.1:c.928_928+1dup
ENST00000706901.1:c.1012_1012+1dup
ENST00000706902.1:c.1012_1012+1dup
ENST00000706903.1:c.1012_1012+1dup
ENST00000706904.1:c.1012_1012+1dup
ENST00000706905.1:c.1012_1012+1dup
ENST00000376809.10:c.1012_1012+1dup
ENST00000638375.1:c.895+219_895+220dup ENSP00000492789.1:n.895+219_895+220dup
ENST00000376802.2:c.895+219_895+220dup ENSP00000365998.2:n.895+219_895+220dup
ENST00000376806.9:c.1012_1013dup ENSP00000366002.5:p.Gly339ValfsTer5
ENST00000376809.9:c.1012_1012+1dup
ENST00000396634.5:c.1012_1012+1dup
ENST00000461903.1:n.1253_1254dup
ENST00000479320.5:n.1253_1253+1dup
ENST00000495183.5:n.1255_1255+1dup
ENST00000496081.5:n.829_830dup
NM_002116.7:c.1012_1012+1dup
NM_002116.8:c.1012_1012+1dup