Canonical Allele Identifier: CA333053275

Gene: PSMD10

Linked Data

• dbSNP Id: rs778491632
• gnomAD v3: X-108084778-G-A
• gnomAD v4: X-108084778-G-A
• MyVariant Identifiers: chrX:g.107328008G>A (hg19) ; chrX:g.108084778G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084778G>A , CM000685.2:g.108084778G>A	GRCh38
NC_000023.10:g.107328008G>A , CM000685.1:g.107328008G>A	GRCh37
NC_000023.9:g.107214664G>A	NCBI36
NG_012521.1:g.11841C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*196C>T MANE Select	ENSP00000217958.3:n.*196C>T
ENST00000217958.7:c.*196C>T	ENSP00000217958.3:n.*196C>T
ENST00000372295.5:c.*196C>T	ENSP00000361369.1:n.*196C>T
ENST00000372296.5:c.*342C>T	ENSP00000361370.1:n.*342C>T
NM_002814.3:c.*196C>T	NP_002805.1:n.*196C>T
NM_170750.2:c.*342C>T	NP_736606.1:n.*342C>T
NM_002814.4:c.*196C>T MANE Select	NP_002805.1:n.*196C>T
NM_170750.3:c.*342C>T	NP_736606.1:n.*342C>T