Canonical Allele Identifier: CA2579673971
Gene: PSMD10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084934del , CM000685.2:g.108084934del GRCh38
NC_000023.10:g.107328164del , CM000685.1:g.107328164del GRCh37
NC_000023.9:g.107214820del NCBI36
NG_012521.1:g.11685del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*40del MANE Select ENSP00000217958.3:n.*40del
ENST00000217958.7:c.*40del ENSP00000217958.3:n.*40del
ENST00000340200.5:c.622del ENSP00000345963.5:n.622del
ENST00000361815.9:c.*186del ENSP00000354906.5:n.*186del
ENST00000372295.5:c.*40del ENSP00000361369.1:n.*40del
ENST00000372296.5:c.*186del ENSP00000361370.1:n.*186del
NM_002814.3:c.*40del NP_002805.1:n.*40del
NM_170750.2:c.*186del NP_736606.1:n.*186del
NM_002814.4:c.*40del MANE Select NP_002805.1:n.*40del
NM_170750.3:c.*186del NP_736606.1:n.*186del
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