Canonical Allele Identifier: CA2450520332

Gene: PSMD10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085056A= , CM000685.2:g.108085056A=	GRCh38
NC_000023.10:g.107328286A= , CM000685.1:g.107328286A=	GRCh37
NC_000023.9:g.107214942A=	NCBI36
NG_012521.1:g.11563T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.599T= MANE Select	ENSP00000217958.3:p.Ile200=
ENST00000217958.7:c.599T=	ENSP00000217958.3:p.Ile200=
ENST00000340200.5:c.500T=	ENSP00000345963.5:p.Ile167=
ENST00000361815.9:c.*64T=	ENSP00000354906.5:n.*64T=
ENST00000372295.5:c.476T=	ENSP00000361369.1:p.Ile159=
ENST00000372296.5:c.*64T=	ENSP00000361370.1:n.*64T=
NM_002814.3:c.599T=	NP_002805.1:p.Ile200=
NM_170750.2:c.*64T=	NP_736606.1:n.*64T=
NM_002814.4:c.599T= MANE Select	NP_002805.1:p.Ile200=
NM_170750.3:c.*64T=	NP_736606.1:n.*64T=