Canonical Allele Identifier: CA658420122
Gene: PSMD10 HGNC NCBI

Linked Data

COSMIC: COSN18957179 COSN18957180
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084808_108084809insT , CM000685.2:g.108084808_108084809insT GRCh38
NC_000023.10:g.107328038_107328039insT , CM000685.1:g.107328038_107328039insT GRCh37
NC_000023.9:g.107214694_107214695insT NCBI36
NG_012521.1:g.11810_11811insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*165_*166insA MANE Select ENSP00000217958.3:n.*165_*166insA
ENST00000217958.7:c.*165_*166insA ENSP00000217958.3:n.*165_*166insA
ENST00000372295.5:c.*165_*166insA ENSP00000361369.1:n.*165_*166insA
ENST00000372296.5:c.*311_*312insA ENSP00000361370.1:n.*311_*312insA
NM_002814.3:c.*165_*166insA NP_002805.1:n.*165_*166insA
NM_170750.2:c.*311_*312insA NP_736606.1:n.*311_*312insA
NM_002814.4:c.*165_*166insA MANE Select NP_002805.1:n.*165_*166insA
NM_170750.3:c.*311_*312insA NP_736606.1:n.*311_*312insA
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