Canonical Allele Identifier: CA1136170211

Gene: PSMD10

Linked Data

• dbSNP Id: rs2031477784
• gnomAD v3: X-108084893-T-C
• gnomAD v4: X-108084893-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084893T>C , CM000685.2:g.108084893T>C	GRCh38
NC_000023.10:g.107328123T>C , CM000685.1:g.107328123T>C	GRCh37
NC_000023.9:g.107214779T>C	NCBI36
NG_012521.1:g.11726A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*81A>G MANE Select	ENSP00000217958.3:n.*81A>G
ENST00000217958.7:c.*81A>G	ENSP00000217958.3:n.*81A>G
ENST00000340200.5:c.663A>G	ENSP00000345963.5:n.663A>G
ENST00000361815.9:c.*227A>G	ENSP00000354906.5:n.*227A>G
ENST00000372295.5:c.*81A>G	ENSP00000361369.1:n.*81A>G
ENST00000372296.5:c.*227A>G	ENSP00000361370.1:n.*227A>G
NM_002814.3:c.*81A>G	NP_002805.1:n.*81A>G
NM_170750.2:c.*227A>G	NP_736606.1:n.*227A>G
NM_002814.4:c.*81A>G MANE Select	NP_002805.1:n.*81A>G
NM_170750.3:c.*227A>G	NP_736606.1:n.*227A>G