Canonical Allele Identifier: CA517921237

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328348G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085118G>T , CM000685.2:g.108085118G>T	GRCh38
NC_000023.10:g.107328348G>T , CM000685.1:g.107328348G>T	GRCh37
NC_000023.9:g.107215004G>T	NCBI36
NG_012521.1:g.11501C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.537C>A MANE Select	ENSP00000217958.3:p.Ala179=
ENST00000217958.7:c.537C>A	ENSP00000217958.3:p.Ala179=
ENST00000340200.5:c.438C>A	ENSP00000345963.5:p.Ala146=
ENST00000361815.9:c.*2C>A	ENSP00000354906.5:n.*2C>A
ENST00000372295.5:c.414C>A	ENSP00000361369.1:p.Ala138=
ENST00000372296.5:c.*2C>A	ENSP00000361370.1:n.*2C>A
NM_002814.3:c.537C>A	NP_002805.1:p.Ala179=
NM_170750.2:c.*2C>A	NP_736606.1:n.*2C>A
NM_002814.4:c.537C>A MANE Select	NP_002805.1:p.Ala179=
NM_170750.3:c.*2C>A	NP_736606.1:n.*2C>A