Canonical Allele Identifier: CA2694424279
Gene: PSMD10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084942_108084946del , CM000685.2:g.108084942_108084946del GRCh38
NC_000023.10:g.107328172_107328176del , CM000685.1:g.107328172_107328176del GRCh37
NC_000023.9:g.107214828_107214832del NCBI36
NG_012521.1:g.11679_11683del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*34_*38del MANE Select ENSP00000217958.3:n.*34_*38del
ENST00000217958.7:c.*34_*38del ENSP00000217958.3:n.*34_*38del
ENST00000340200.5:c.616_620del ENSP00000345963.5:n.616_620del
ENST00000361815.9:c.*180_*184del ENSP00000354906.5:n.*180_*184del
ENST00000372295.5:c.*34_*38del ENSP00000361369.1:n.*34_*38del
ENST00000372296.5:c.*180_*184del ENSP00000361370.1:n.*180_*184del
NM_002814.3:c.*34_*38del NP_002805.1:n.*34_*38del
NM_170750.2:c.*180_*184del NP_736606.1:n.*180_*184del
NM_002814.4:c.*34_*38del MANE Select NP_002805.1:n.*34_*38del
NM_170750.3:c.*180_*184del NP_736606.1:n.*180_*184del