Canonical Allele Identifier: CA1619077135

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31268884T= , CM000668.2:g.31268884T=	GRCh38
NC_000006.11:g.31236661T= , CM000668.1:g.31236661T=	GRCh37
NC_000006.10:g.31344640T=	NCBI36
NG_029422.2:g.8248A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.*285A= MANE Select	ENSP00000365402.5:n.*285A=
ENST00000376228.9:c.*285A=	ENSP00000365402.5:n.*285A=
ENST00000376237.8:c.*973A=	ENSP00000365412.4:n.*973A=
ENST00000383329.7:c.*285A=	ENSP00000372819.3:n.*285A=
ENST00000466892.5:n.619A=
ENST00000470363.5:n.1144A=
ENST00000487245.5:n.1745A=
NM_002117.5:c.*285A=	NP_002108.4:n.*285A=
NM_002117.6:c.*285A= MANE Select	NP_002108.4:n.*285A=