Canonical Allele Identifier: CA1619080477

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271279T= , CM000668.2:g.31271279T=	GRCh38
NC_000006.11:g.31239056T= , CM000668.1:g.31239056T=	GRCh37
NC_000006.10:g.31347035T=	NCBI36
NG_029422.2:g.5853A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.413A= MANE Select	ENSP00000365402.5:p.Asp138=
ENST00000376228.9:c.413A=	ENSP00000365402.5:p.Asp138=
ENST00000376237.8:c.396A=	ENSP00000365412.4:p.Ter132=
ENST00000383329.7:c.413A=	ENSP00000372819.3:p.Asp138=
ENST00000415537.1:c.411A=
ENST00000484378.1:n.682A=
ENST00000487245.5:n.772A=
ENST00000495835.1:n.602A=
NM_002117.5:c.413A=	NP_002108.4:p.Asp138=
NM_002117.6:c.413A= MANE Select	NP_002108.4:p.Asp138=