Canonical Allele Identifier: CA517921142

Gene: PSMD10

Linked Data

• gnomAD v4: X-108084927-C-T
• MyVariant Identifiers: chrX:g.107328157C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084927C>T , CM000685.2:g.108084927C>T	GRCh38
NC_000023.10:g.107328157C>T , CM000685.1:g.107328157C>T	GRCh37
NC_000023.9:g.107214813C>T	NCBI36
NG_012521.1:g.11692G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*47G>A MANE Select	ENSP00000217958.3:n.*47G>A
ENST00000217958.7:c.*47G>A	ENSP00000217958.3:n.*47G>A
ENST00000340200.5:c.629G>A	ENSP00000345963.5:n.629G>A
ENST00000361815.9:c.*193G>A	ENSP00000354906.5:n.*193G>A
ENST00000372295.5:c.*47G>A	ENSP00000361369.1:n.*47G>A
ENST00000372296.5:c.*193G>A	ENSP00000361370.1:n.*193G>A
NM_002814.3:c.*47G>A	NP_002805.1:n.*47G>A
NM_170750.2:c.*193G>A	NP_736606.1:n.*193G>A
NM_002814.4:c.*47G>A MANE Select	NP_002805.1:n.*47G>A
NM_170750.3:c.*193G>A	NP_736606.1:n.*193G>A