Canonical Allele Identifier: CA517921163

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328234A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085004A>T , CM000685.2:g.108085004A>T	GRCh38
NC_000023.10:g.107328234A>T , CM000685.1:g.107328234A>T	GRCh37
NC_000023.9:g.107214890A>T	NCBI36
NG_012521.1:g.11615T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.651T>A MANE Select	ENSP00000217958.3:p.Gly217=
ENST00000217958.7:c.651T>A	ENSP00000217958.3:p.Gly217=
ENST00000340200.5:c.552T>A	ENSP00000345963.5:p.Gly184=
ENST00000361815.9:c.*116T>A	ENSP00000354906.5:n.*116T>A
ENST00000372295.5:c.528T>A	ENSP00000361369.1:p.Gly176=
ENST00000372296.5:c.*116T>A	ENSP00000361370.1:n.*116T>A
NM_002814.3:c.651T>A	NP_002805.1:p.Gly217=
NM_170750.2:c.*116T>A	NP_736606.1:n.*116T>A
NM_002814.4:c.651T>A MANE Select	NP_002805.1:p.Gly217=
NM_170750.3:c.*116T>A	NP_736606.1:n.*116T>A