Canonical Allele Identifier: CA1619080387

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271180A= , CM000668.2:g.31271180A=	GRCh38
NC_000006.11:g.31238957A= , CM000668.1:g.31238957A=	GRCh37
NC_000006.10:g.31346936A=	NCBI36
NG_029422.2:g.5952T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.512T= MANE Select	ENSP00000365402.5:p.Leu171=
ENST00000376228.9:c.512T=	ENSP00000365402.5:p.Leu171=
ENST00000376237.8:c.*99T=	ENSP00000365412.4:n.*99T=
ENST00000383329.7:c.512T=	ENSP00000372819.3:p.Leu171=
ENST00000415537.1:c.510T=
ENST00000484378.1:n.781T=
ENST00000487245.5:n.871T=
ENST00000495835.1:n.701T=
NM_002117.5:c.512T=	NP_002108.4:p.Leu171=
NM_002117.6:c.512T= MANE Select	NP_002108.4:p.Leu171=