Canonical Allele Identifier: CA2450520312

Gene: PSMD10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084978C= , CM000685.2:g.108084978C=	GRCh38
NC_000023.10:g.107328208C= , CM000685.1:g.107328208C=	GRCh37
NC_000023.9:g.107214864C=	NCBI36
NG_012521.1:g.11641G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.677G= MANE Select	ENSP00000217958.3:p.Gly226=
ENST00000217958.7:c.677G=	ENSP00000217958.3:p.Gly226=
ENST00000340200.5:c.578G=	ENSP00000345963.5:p.Gly193=
ENST00000361815.9:c.*142G=	ENSP00000354906.5:n.*142G=
ENST00000372295.5:c.554G=	ENSP00000361369.1:p.Gly185=
ENST00000372296.5:c.*142G=	ENSP00000361370.1:n.*142G=
NM_002814.3:c.677G=	NP_002805.1:p.Gly226=
NM_170750.2:c.*142G=	NP_736606.1:n.*142G=
NM_002814.4:c.677G= MANE Select	NP_002805.1:p.Gly226=
NM_170750.3:c.*142G=	NP_736606.1:n.*142G=