Canonical Allele Identifier: CA1619080337

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271129C= , CM000668.2:g.31271129C=	GRCh38
NC_000006.11:g.31238906C= , CM000668.1:g.31238906C=	GRCh37
NC_000006.10:g.31346885C=	NCBI36
NG_029422.2:g.6003G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.563G= MANE Select	ENSP00000365402.5:p.Cys188=
ENST00000376228.9:c.563G=	ENSP00000365402.5:p.Cys188=
ENST00000376237.8:c.*150G=	ENSP00000365412.4:n.*150G=
ENST00000383329.7:c.563G=	ENSP00000372819.3:p.Cys188=
ENST00000415537.1:c.561G=
ENST00000484378.1:n.832G=
ENST00000487245.5:n.922G=
ENST00000495835.1:n.752G=
NM_002117.5:c.563G=	NP_002108.4:p.Cys188=
NM_002117.6:c.563G= MANE Select	NP_002108.4:p.Cys188=