Canonical Allele Identifier: CA2694424264
Gene: PSMD10 HGNC NCBI

Linked Data

gnomAD v4: X-108084899-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084899G>T , CM000685.2:g.108084899G>T GRCh38
NC_000023.10:g.107328129G>T , CM000685.1:g.107328129G>T GRCh37
NC_000023.9:g.107214785G>T NCBI36
NG_012521.1:g.11720C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*75C>A MANE Select ENSP00000217958.3:n.*75C>A
ENST00000217958.7:c.*75C>A ENSP00000217958.3:n.*75C>A
ENST00000340200.5:c.657C>A ENSP00000345963.5:n.657C>A
ENST00000361815.9:c.*221C>A ENSP00000354906.5:n.*221C>A
ENST00000372295.5:c.*75C>A ENSP00000361369.1:n.*75C>A
ENST00000372296.5:c.*221C>A ENSP00000361370.1:n.*221C>A
NM_002814.3:c.*75C>A NP_002805.1:n.*75C>A
NM_170750.2:c.*221C>A NP_736606.1:n.*221C>A
NM_002814.4:c.*75C>A MANE Select NP_002805.1:n.*75C>A
NM_170750.3:c.*221C>A NP_736606.1:n.*221C>A
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