Canonical Allele Identifier: CA2579673972
Gene: PSMD10 HGNC NCBI

Linked Data

gnomAD v4: X-108084942-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084944del , CM000685.2:g.108084944del GRCh38
NC_000023.10:g.107328174del , CM000685.1:g.107328174del GRCh37
NC_000023.9:g.107214830del NCBI36
NG_012521.1:g.11676del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*31del MANE Select ENSP00000217958.3:n.*31del
ENST00000217958.7:c.*31del ENSP00000217958.3:n.*31del
ENST00000340200.5:c.613del ENSP00000345963.5:n.613del
ENST00000361815.9:c.*177del ENSP00000354906.5:n.*177del
ENST00000372295.5:c.*31del ENSP00000361369.1:n.*31del
ENST00000372296.5:c.*177del ENSP00000361370.1:n.*177del
NM_002814.3:c.*31del NP_002805.1:n.*31del
NM_170750.2:c.*177del NP_736606.1:n.*177del
NM_002814.4:c.*31del MANE Select NP_002805.1:n.*31del
NM_170750.3:c.*177del NP_736606.1:n.*177del
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