Canonical Allele Identifier: CA1619080468

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271271C= , CM000668.2:g.31271271C=	GRCh38
NC_000006.11:g.31239048C= , CM000668.1:g.31239048C=	GRCh37
NC_000006.10:g.31347027C=	NCBI36
NG_029422.2:g.5861G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.421G= MANE Select	ENSP00000365402.5:p.Ala141=
ENST00000376228.9:c.421G=	ENSP00000365402.5:p.Ala141=
ENST00000376237.8:c.*8G=	ENSP00000365412.4:n.*8G=
ENST00000383329.7:c.421G=	ENSP00000372819.3:p.Ala141=
ENST00000415537.1:c.419G=
ENST00000484378.1:n.690G=
ENST00000487245.5:n.780G=
ENST00000495835.1:n.610G=
NM_002117.5:c.421G=	NP_002108.4:p.Ala141=
NM_002117.6:c.421G= MANE Select	NP_002108.4:p.Ala141=