Canonical Allele Identifier: CA413841803

Gene: PSMD10

Linked Data

• gnomAD v4: X-108085119-G-C
• MyVariant Identifiers: chrX:g.107328349G>C (hg19) ; chrX:g.108085119G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085119G>C , CM000685.2:g.108085119G>C	GRCh38
NC_000023.10:g.107328349G>C , CM000685.1:g.107328349G>C	GRCh37
NC_000023.9:g.107215005G>C	NCBI36
NG_012521.1:g.11500C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.536C>G MANE Select	ENSP00000217958.3:p.Ala179Gly
ENST00000217958.7:c.536C>G	ENSP00000217958.3:p.Ala179Gly
ENST00000340200.5:c.437C>G	ENSP00000345963.5:p.Ala146Gly
ENST00000361815.9:c.*1C>G	ENSP00000354906.5:n.*1C>G
ENST00000372295.5:c.413C>G	ENSP00000361369.1:p.Ala138Gly
ENST00000372296.5:c.*1C>G	ENSP00000361370.1:n.*1C>G
NM_002814.3:c.536C>G	NP_002805.1:p.Ala179Gly
NM_170750.2:c.*1C>G	NP_736606.1:n.*1C>G
NM_002814.4:c.536C>G MANE Select	NP_002805.1:p.Ala179Gly
NM_170750.3:c.*1C>G	NP_736606.1:n.*1C>G