Canonical Allele Identifier: CA1618521122

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945851A= , CM000668.2:g.29945851A=	GRCh38
NC_000006.11:g.29913628A= , CM000668.1:g.29913628A=	GRCh37
NC_000006.10:g.30021607A=	NCBI36
NG_029217.2:g.8387A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1377A=	ENSP00000492789.2:n.1377A=
ENST00000706899.1:n.2348A=
ENST00000706900.1:c.*396A=	ENSP00000516617.1:n.*396A=
ENST00000706901.1:c.*396A=	ENSP00000516612.1:n.*396A=
ENST00000706902.1:c.1093+570A=	ENSP00000516613.1:n.1093+570A=
ENST00000706903.1:c.*124+272A=	ENSP00000516614.1:n.*124+272A=
ENST00000706904.1:c.1093+570A=	ENSP00000516615.1:n.1093+570A=
ENST00000706905.1:c.*396A=	ENSP00000516616.1:n.*396A=
ENST00000376809.10:c.*396A= MANE Select	ENSP00000366005.5:n.*396A=
ENST00000376802.2:c.*396A=	ENSP00000365998.2:n.*396A=
ENST00000376806.9:c.*396A=	ENSP00000366002.5:n.*396A=
ENST00000376809.9:c.*396A=	ENSP00000366005.5:n.*396A=
ENST00000396634.5:c.*396A=	ENSP00000379873.1:n.*396A=
ENST00000495183.5:n.1733A=
ENST00000496081.5:n.1753A=
NM_002116.7:c.*396A=	NP_002107.3:n.*396A=
NM_002116.8:c.*396A= MANE Select	NP_002107.3:n.*396A=