Canonical Allele Identifier: CA1618520783

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945496C= , CM000668.2:g.29945496C=	GRCh38
NC_000006.11:g.29913273C= , CM000668.1:g.29913273C=	GRCh37
NC_000006.10:g.30021252C=	NCBI36
NG_029217.2:g.8032C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1022C=	ENSP00000492789.2:n.1022C=
ENST00000706892.1:n.2848C=
ENST00000706893.1:c.*123C=	ENSP00000516609.1:n.*123C=
ENST00000706894.1:c.*123C=	ENSP00000516610.1:n.*123C=
ENST00000706895.1:n.2128C=
ENST00000706896.1:n.2435C=
ENST00000706897.1:n.1857C=
ENST00000706898.1:c.*41C=	ENSP00000516611.1:n.*41C=
ENST00000706899.1:n.1993C=
ENST00000706900.1:c.*41C=	ENSP00000516617.1:n.*41C=
ENST00000706901.1:c.*41C=	ENSP00000516612.1:n.*41C=
ENST00000706902.1:c.1093+215C=	ENSP00000516613.1:n.1093+215C=
ENST00000706903.1:c.*41C=	ENSP00000516614.1:n.*41C=
ENST00000706904.1:c.1093+215C=	ENSP00000516615.1:n.1093+215C=
ENST00000706905.1:c.*41C=	ENSP00000516616.1:n.*41C=
ENST00000376809.10:c.*41C= MANE Select	ENSP00000366005.5:n.*41C=
ENST00000376802.2:c.*41C=	ENSP00000365998.2:n.*41C=
ENST00000376806.9:c.*41C=	ENSP00000366002.5:n.*41C=
ENST00000376809.9:c.*41C=	ENSP00000366005.5:n.*41C=
ENST00000396634.5:c.*41C=	ENSP00000379873.1:n.*41C=
ENST00000495183.5:n.1378C=
ENST00000496081.5:n.1398C=
NM_002116.7:c.*41C=	NP_002107.3:n.*41C=
NM_002116.8:c.*41C= MANE Select	NP_002107.3:n.*41C=