Canonical Allele Identifier: CA658420118
Gene: PSMD10 HGNC NCBI

Linked Data

COSMIC: COSN22995040
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084580_108084581insC , CM000685.2:g.108084580_108084581insC GRCh38
NC_000023.10:g.107327810_107327811insC , CM000685.1:g.107327810_107327811insC GRCh37
NC_000023.9:g.107214466_107214467insC NCBI36
NG_012521.1:g.12038_12039insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*393_*394insG MANE Select ENSP00000217958.3:n.*393_*394insG
ENST00000217958.7:c.*393_*394insG ENSP00000217958.3:n.*393_*394insG
NM_002814.3:c.*393_*394insG NP_002805.1:n.*393_*394insG
NM_170750.2:c.*539_*540insG NP_736606.1:n.*539_*540insG
NM_002814.4:c.*393_*394insG MANE Select NP_002805.1:n.*393_*394insG
NM_170750.3:c.*539_*540insG NP_736606.1:n.*539_*540insG
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Search 100 bp 3'