Canonical Allele Identifier: CA1136170234

Gene: PSMD10

Linked Data

• dbSNP Id: rs2031478056
• gnomAD v3: X-108084920-T-C
• gnomAD v4: X-108084920-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084920T>C , CM000685.2:g.108084920T>C	GRCh38
NC_000023.10:g.107328150T>C , CM000685.1:g.107328150T>C	GRCh37
NC_000023.9:g.107214806T>C	NCBI36
NG_012521.1:g.11699A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000217958.8:c.*54A>G MANE Select	ENSP00000217958.3:n.*54A>G
ENST00000217958.7:c.*54A>G	ENSP00000217958.3:n.*54A>G
ENST00000340200.5:c.636A>G	ENSP00000345963.5:n.636A>G
ENST00000361815.9:c.*200A>G	ENSP00000354906.5:n.*200A>G
ENST00000372295.5:c.*54A>G	ENSP00000361369.1:n.*54A>G
ENST00000372296.5:c.*200A>G	ENSP00000361370.1:n.*200A>G
NM_002814.3:c.*54A>G	NP_002805.1:n.*54A>G
NM_170750.2:c.*200A>G	NP_736606.1:n.*200A>G
NM_002814.4:c.*54A>G MANE Select	NP_002805.1:n.*54A>G
NM_170750.3:c.*200A>G	NP_736606.1:n.*200A>G