Canonical Allele Identifier: CA1618520932

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945602C= , CM000668.2:g.29945602C=	GRCh38
NC_000006.11:g.29913379C= , CM000668.1:g.29913379C=	GRCh37
NC_000006.10:g.30021358C=	NCBI36
NG_029217.2:g.8138C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1128C=	ENSP00000492789.2:n.1128C=
ENST00000706892.1:n.2954C=
ENST00000706893.1:c.*229C=	ENSP00000516609.1:n.*229C=
ENST00000706894.1:c.*229C=	ENSP00000516610.1:n.*229C=
ENST00000706895.1:n.2234C=
ENST00000706896.1:n.2541C=
ENST00000706897.1:n.1963C=
ENST00000706898.1:c.*147C=	ENSP00000516611.1:n.*147C=
ENST00000706899.1:n.2099C=
ENST00000706900.1:c.*147C=	ENSP00000516617.1:n.*147C=
ENST00000706901.1:c.*147C=	ENSP00000516612.1:n.*147C=
ENST00000706902.1:c.1093+321C=	ENSP00000516613.1:n.1093+321C=
ENST00000706903.1:c.*124+23C=	ENSP00000516614.1:n.*124+23C=
ENST00000706904.1:c.1093+321C=	ENSP00000516615.1:n.1093+321C=
ENST00000706905.1:c.*147C=	ENSP00000516616.1:n.*147C=
ENST00000376809.10:c.*147C= MANE Select	ENSP00000366005.5:n.*147C=
ENST00000376802.2:c.*147C=	ENSP00000365998.2:n.*147C=
ENST00000376806.9:c.*147C=	ENSP00000366002.5:n.*147C=
ENST00000376809.9:c.*147C=	ENSP00000366005.5:n.*147C=
ENST00000396634.5:c.*147C=	ENSP00000379873.1:n.*147C=
ENST00000495183.5:n.1484C=
ENST00000496081.5:n.1504C=
NM_002116.7:c.*147C=	NP_002107.3:n.*147C=
NM_002116.8:c.*147C= MANE Select	NP_002107.3:n.*147C=