Canonical Allele Identifier: CA658420130

Gene: PSMD10

Linked Data

• COSMIC: COSN2336541

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084895del , CM000685.2:g.108084895del	GRCh38
NC_000023.10:g.107328125del , CM000685.1:g.107328125del	GRCh37
NC_000023.9:g.107214781del	NCBI36
NG_012521.1:g.11724del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*79del MANE Select	ENSP00000217958.3:n.*79del
ENST00000217958.7:c.*79del	ENSP00000217958.3:n.*79del
ENST00000340200.5:c.661del	ENSP00000345963.5:n.661del
ENST00000361815.9:c.*225del	ENSP00000354906.5:n.*225del
ENST00000372295.5:c.*79del	ENSP00000361369.1:n.*79del
ENST00000372296.5:c.*225del	ENSP00000361370.1:n.*225del
NM_002814.3:c.*79del	NP_002805.1:n.*79del
NM_170750.2:c.*225del	NP_736606.1:n.*225del
NM_002814.4:c.*79del MANE Select	NP_002805.1:n.*79del
NM_170750.3:c.*225del	NP_736606.1:n.*225del