Canonical Allele Identifier: CA1619077742

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269365A= , CM000668.2:g.31269365A=	GRCh38
NC_000006.11:g.31237142A= , CM000668.1:g.31237142A=	GRCh37
NC_000006.10:g.31345121A=	NCBI36
NG_029422.2:g.7767T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.1069T= MANE Select	ENSP00000365402.5:p.Ser357=
ENST00000376228.9:c.1069T=	ENSP00000365402.5:p.Ser357=
ENST00000376237.8:c.*656T=	ENSP00000365412.4:n.*656T=
ENST00000383329.7:c.1087T=	ENSP00000372819.3:p.Ser363=
ENST00000466892.5:n.302T=
ENST00000470363.5:n.827T=
ENST00000487245.5:n.1428T=
NM_002117.5:c.1069T=	NP_002108.4:p.Ser357=
NM_002117.6:c.1069T= MANE Select	NP_002108.4:p.Ser357=