Canonical Allele Identifier: CA1619080168

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270836A= , CM000668.2:g.31270836A=	GRCh38
NC_000006.11:g.31238613A= , CM000668.1:g.31238613A=	GRCh37
NC_000006.10:g.31346592A=	NCBI36
NG_029422.2:g.6296T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.619+237T= MANE Select	ENSP00000365402.5:n.619+237T=
ENST00000376228.9:c.619+237T=	ENSP00000365402.5:n.619+237T=
ENST00000376237.8:c.*206+237T=	ENSP00000365412.4:n.*206+237T=
ENST00000383329.7:c.619+237T=	ENSP00000372819.3:n.619+237T=
ENST00000415537.1:c.617+237T=
ENST00000487245.5:n.978+237T=
ENST00000495835.1:n.808+237T=
NM_002117.5:c.619+237T=	NP_002108.4:n.619+237T=
NM_002117.6:c.619+237T= MANE Select	NP_002108.4:n.619+237T=