Canonical Allele Identifier: CA1619080403

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271193T= , CM000668.2:g.31271193T=	GRCh38
NC_000006.11:g.31238970T= , CM000668.1:g.31238970T=	GRCh37
NC_000006.10:g.31346949T=	NCBI36
NG_029422.2:g.5939A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.499A= MANE Select	ENSP00000365402.5:p.Thr167=
ENST00000376228.9:c.499A=	ENSP00000365402.5:p.Thr167=
ENST00000376237.8:c.*86A=	ENSP00000365412.4:n.*86A=
ENST00000383329.7:c.499A=	ENSP00000372819.3:p.Thr167=
ENST00000415537.1:c.497A=
ENST00000484378.1:n.768A=
ENST00000487245.5:n.858A=
ENST00000495835.1:n.688A=
NM_002117.5:c.499A=	NP_002108.4:p.Thr167=
NM_002117.6:c.499A= MANE Select	NP_002108.4:p.Thr167=