Canonical Allele Identifier: CA1619080342

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271132G= , CM000668.2:g.31271132G=	GRCh38
NC_000006.11:g.31238909G= , CM000668.1:g.31238909G=	GRCh37
NC_000006.10:g.31346888G=	NCBI36
NG_029422.2:g.6000C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.560C= MANE Select	ENSP00000365402.5:p.Thr187=
ENST00000376228.9:c.560C=	ENSP00000365402.5:p.Thr187=
ENST00000376237.8:c.*147C=	ENSP00000365412.4:n.*147C=
ENST00000383329.7:c.560C=	ENSP00000372819.3:p.Thr187=
ENST00000415537.1:c.558C=
ENST00000484378.1:n.829C=
ENST00000487245.5:n.919C=
ENST00000495835.1:n.749C=
NM_002117.5:c.560C=	NP_002108.4:p.Thr187=
NM_002117.6:c.560C= MANE Select	NP_002108.4:p.Thr187=