Canonical Allele Identifier: CA1619077124

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31268866T= , CM000668.2:g.31268866T=	GRCh38
NC_000006.11:g.31236643T= , CM000668.1:g.31236643T=	GRCh37
NC_000006.10:g.31344622T=	NCBI36
NG_029422.2:g.8266A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.*303A= MANE Select	ENSP00000365402.5:n.*303A=
ENST00000376228.9:c.*303A=	ENSP00000365402.5:n.*303A=
ENST00000376237.8:c.*991A=	ENSP00000365412.4:n.*991A=
ENST00000383329.7:c.*303A=	ENSP00000372819.3:n.*303A=
ENST00000466892.5:n.637A=
ENST00000470363.5:n.1162A=
ENST00000487245.5:n.1763A=
NM_002117.5:c.*303A=	NP_002108.4:n.*303A=
NM_002117.6:c.*303A= MANE Select	NP_002108.4:n.*303A=