Canonical Allele Identifier: CA10486657

Gene: PSMD10

Linked Data

• dbSNP Id: rs756260381
• ExAC: X:107328153 G / A
• gnomAD v2: X-107328153-G-A
• gnomAD v4: X-108084923-G-A
• MyVariant Identifiers: chrX:g.107328153G>A (hg19) ; chrX:g.108084923G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084923G>A , CM000685.2:g.108084923G>A	GRCh38
NC_000023.10:g.107328153G>A , CM000685.1:g.107328153G>A	GRCh37
NC_000023.9:g.107214809G>A	NCBI36
NG_012521.1:g.11696C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*51C>T MANE Select	ENSP00000217958.3:n.*51C>T
ENST00000217958.7:c.*51C>T	ENSP00000217958.3:n.*51C>T
ENST00000340200.5:c.633C>T	ENSP00000345963.5:n.633C>T
ENST00000361815.9:c.*197C>T	ENSP00000354906.5:n.*197C>T
ENST00000372295.5:c.*51C>T	ENSP00000361369.1:n.*51C>T
ENST00000372296.5:c.*197C>T	ENSP00000361370.1:n.*197C>T
NM_002814.3:c.*51C>T	NP_002805.1:n.*51C>T
NM_170750.2:c.*197C>T	NP_736606.1:n.*197C>T
NM_002814.4:c.*51C>T MANE Select	NP_002805.1:n.*51C>T
NM_170750.3:c.*197C>T	NP_736606.1:n.*197C>T