Canonical Allele Identifier: CA1618521100

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945797T= , CM000668.2:g.29945797T=	GRCh38
NC_000006.11:g.29913574T= , CM000668.1:g.29913574T=	GRCh37
NC_000006.10:g.30021553T=	NCBI36
NG_029217.2:g.8333T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1323T=	ENSP00000492789.2:n.1323T=
ENST00000706896.1:n.2736T=
ENST00000706897.1:n.2158T=
ENST00000706898.1:c.*342T=	ENSP00000516611.1:n.*342T=
ENST00000706899.1:n.2294T=
ENST00000706900.1:c.*342T=	ENSP00000516617.1:n.*342T=
ENST00000706901.1:c.*342T=	ENSP00000516612.1:n.*342T=
ENST00000706902.1:c.1093+516T=	ENSP00000516613.1:n.1093+516T=
ENST00000706903.1:c.*124+218T=	ENSP00000516614.1:n.*124+218T=
ENST00000706904.1:c.1093+516T=	ENSP00000516615.1:n.1093+516T=
ENST00000706905.1:c.*342T=	ENSP00000516616.1:n.*342T=
ENST00000376809.10:c.*342T= MANE Select	ENSP00000366005.5:n.*342T=
ENST00000376802.2:c.*342T=	ENSP00000365998.2:n.*342T=
ENST00000376806.9:c.*342T=	ENSP00000366002.5:n.*342T=
ENST00000376809.9:c.*342T=	ENSP00000366005.5:n.*342T=
ENST00000396634.5:c.*342T=	ENSP00000379873.1:n.*342T=
ENST00000495183.5:n.1679T=
ENST00000496081.5:n.1699T=
NM_002116.7:c.*342T=	NP_002107.3:n.*342T=
NM_002116.8:c.*342T= MANE Select	NP_002107.3:n.*342T=