Canonical Allele Identifier: CA1619079242

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270185T= , CM000668.2:g.31270185T=	GRCh38
NC_000006.11:g.31237962T= , CM000668.1:g.31237962T=	GRCh37
NC_000006.10:g.31345941T=	NCBI36
NG_029422.2:g.6947A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.895+25A= MANE Select	ENSP00000365402.5:n.895+25A=
ENST00000376228.9:c.895+25A=	ENSP00000365402.5:n.895+25A=
ENST00000376237.8:c.*482+25A=	ENSP00000365412.4:n.*482+25A=
ENST00000383329.7:c.895+25A=	ENSP00000372819.3:n.895+25A=
ENST00000470363.5:n.213+25A=
ENST00000487245.5:n.1254+25A=
NM_002117.5:c.895+25A=	NP_002108.4:n.895+25A=
NM_002117.6:c.895+25A= MANE Select	NP_002108.4:n.895+25A=