Canonical Allele Identifier: CA1136170199
Gene: PSMD10 HGNC NCBI

Linked Data

dbSNP Id: rs2031476790
gnomAD v3: X-108084813-G-A
gnomAD v4: X-108084813-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084813G>A , CM000685.2:g.108084813G>A GRCh38
NC_000023.10:g.107328043G>A , CM000685.1:g.107328043G>A GRCh37
NC_000023.9:g.107214699G>A NCBI36
NG_012521.1:g.11806C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000217958.8:c.*161C>T MANE Select ENSP00000217958.3:n.*161C>T
ENST00000217958.7:c.*161C>T ENSP00000217958.3:n.*161C>T
ENST00000372295.5:c.*161C>T ENSP00000361369.1:n.*161C>T
ENST00000372296.5:c.*307C>T ENSP00000361370.1:n.*307C>T
NM_002814.3:c.*161C>T NP_002805.1:n.*161C>T
NM_170750.2:c.*307C>T NP_736606.1:n.*307C>T
NM_002814.4:c.*161C>T MANE Select NP_002805.1:n.*161C>T
NM_170750.3:c.*307C>T NP_736606.1:n.*307C>T
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