Canonical Allele Identifier: CA1619079962

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270484T= , CM000668.2:g.31270484T=	GRCh38
NC_000006.11:g.31238261T= , CM000668.1:g.31238261T=	GRCh37
NC_000006.10:g.31346240T=	NCBI36
NG_029422.2:g.6648A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.621A= MANE Select	ENSP00000365402.5:p.Glu207=
ENST00000376228.9:c.621A=	ENSP00000365402.5:p.Glu207=
ENST00000376237.8:c.*208A=	ENSP00000365412.4:n.*208A=
ENST00000383329.7:c.621A=	ENSP00000372819.3:p.Glu207=
ENST00000415537.1:c.619A=
ENST00000487245.5:n.980A=
ENST00000495835.1:n.810A=
NM_002117.5:c.621A=	NP_002108.4:p.Glu207=
NM_002117.6:c.621A= MANE Select	NP_002108.4:p.Glu207=