Canonical Allele Identifier: CA2547093977
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084940_108084942del , CM000685.2:g.108084940_108084942del GRCh38
NC_000023.10:g.107328170_107328172del , CM000685.1:g.107328170_107328172del GRCh37
NC_000023.9:g.107214826_107214828del NCBI36
NG_012521.1:g.11677_11679del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*32_*34del MANE Select ENSP00000217958.3:n.*32_*34del
ENST00000217958.7:c.*32_*34del ENSP00000217958.3:n.*32_*34del
ENST00000340200.5:c.614_616del ENSP00000345963.5:n.614_616del
ENST00000361815.9:c.*178_*180del ENSP00000354906.5:n.*178_*180del
ENST00000372295.5:c.*32_*34del ENSP00000361369.1:n.*32_*34del
ENST00000372296.5:c.*178_*180del ENSP00000361370.1:n.*178_*180del
NM_002814.3:c.*32_*34del NP_002805.1:n.*32_*34del
NM_170750.2:c.*178_*180del NP_736606.1:n.*178_*180del
NM_002814.4:c.*32_*34del MANE Select NP_002805.1:n.*32_*34del
NM_170750.3:c.*178_*180del NP_736606.1:n.*178_*180del