Canonical Allele Identifier: CA2450520267

Gene: PSMD10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084813G= , CM000685.2:g.108084813G=	GRCh38
NC_000023.10:g.107328043G= , CM000685.1:g.107328043G=	GRCh37
NC_000023.9:g.107214699G=	NCBI36
NG_012521.1:g.11806C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000217958.8:c.*161C= MANE Select	ENSP00000217958.3:n.*161C=
ENST00000217958.7:c.*161C=	ENSP00000217958.3:n.*161C=
ENST00000372295.5:c.*161C=	ENSP00000361369.1:n.*161C=
ENST00000372296.5:c.*307C=	ENSP00000361370.1:n.*307C=
NM_002814.3:c.*161C=	NP_002805.1:n.*161C=
NM_170750.2:c.*307C=	NP_736606.1:n.*307C=
NM_002814.4:c.*161C= MANE Select	NP_002805.1:n.*161C=
NM_170750.3:c.*307C=	NP_736606.1:n.*307C=