Canonical Allele Identifier: CA2694424218
Gene: PSMD10 HGNC NCBI

Linked Data

gnomAD v4: X-108084812-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084812C>A , CM000685.2:g.108084812C>A GRCh38
NC_000023.10:g.107328042C>A , CM000685.1:g.107328042C>A GRCh37
NC_000023.9:g.107214698C>A NCBI36
NG_012521.1:g.11807G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*162G>T MANE Select ENSP00000217958.3:n.*162G>T
ENST00000217958.7:c.*162G>T ENSP00000217958.3:n.*162G>T
ENST00000372295.5:c.*162G>T ENSP00000361369.1:n.*162G>T
ENST00000372296.5:c.*308G>T ENSP00000361370.1:n.*308G>T
NM_002814.3:c.*162G>T NP_002805.1:n.*162G>T
NM_170750.2:c.*308G>T NP_736606.1:n.*308G>T
NM_002814.4:c.*162G>T MANE Select NP_002805.1:n.*162G>T
NM_170750.3:c.*308G>T NP_736606.1:n.*308G>T
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Search 100 bp 3'