Canonical Allele Identifier: CA2694424209
Gene: PSMD10 HGNC NCBI

Linked Data

gnomAD v4: X-108084792-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084792G>T , CM000685.2:g.108084792G>T GRCh38
NC_000023.10:g.107328022G>T , CM000685.1:g.107328022G>T GRCh37
NC_000023.9:g.107214678G>T NCBI36
NG_012521.1:g.11827C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*182C>A MANE Select ENSP00000217958.3:n.*182C>A
ENST00000217958.7:c.*182C>A ENSP00000217958.3:n.*182C>A
ENST00000372295.5:c.*182C>A ENSP00000361369.1:n.*182C>A
ENST00000372296.5:c.*328C>A ENSP00000361370.1:n.*328C>A
NM_002814.3:c.*182C>A NP_002805.1:n.*182C>A
NM_170750.2:c.*328C>A NP_736606.1:n.*328C>A
NM_002814.4:c.*182C>A MANE Select NP_002805.1:n.*182C>A
NM_170750.3:c.*328C>A NP_736606.1:n.*328C>A
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