Canonical Allele Identifier: CA1619079696

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270302C= , CM000668.2:g.31270302C=	GRCh38
NC_000006.11:g.31238079C= , CM000668.1:g.31238079C=	GRCh37
NC_000006.10:g.31346058C=	NCBI36
NG_029422.2:g.6830G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.803G= MANE Select	ENSP00000365402.5:p.Trp268=
ENST00000376228.9:c.803G=	ENSP00000365402.5:p.Trp268=
ENST00000376237.8:c.*390G=	ENSP00000365412.4:n.*390G=
ENST00000383329.7:c.803G=	ENSP00000372819.3:p.Trp268=
ENST00000415537.1:c.694G=
ENST00000470363.5:n.121G=
ENST00000487245.5:n.1162G=
ENST00000495835.1:n.992G=
NM_002117.5:c.803G=	NP_002108.4:p.Trp268=
NM_002117.6:c.803G= MANE Select	NP_002108.4:p.Trp268=