Canonical Allele Identifier: CA1619080375

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271165G= , CM000668.2:g.31271165G=	GRCh38
NC_000006.11:g.31238942G= , CM000668.1:g.31238942G=	GRCh37
NC_000006.10:g.31346921G=	NCBI36
NG_029422.2:g.5967C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.527C= MANE Select	ENSP00000365402.5:p.Ala176=
ENST00000376228.9:c.527C=	ENSP00000365402.5:p.Ala176=
ENST00000376237.8:c.*114C=	ENSP00000365412.4:n.*114C=
ENST00000383329.7:c.527C=	ENSP00000372819.3:p.Ala176=
ENST00000415537.1:c.525C=
ENST00000484378.1:n.796C=
ENST00000487245.5:n.886C=
ENST00000495835.1:n.716C=
NM_002117.5:c.527C=	NP_002108.4:p.Ala176=
NM_002117.6:c.527C= MANE Select	NP_002108.4:p.Ala176=