Canonical Allele Identifier: CA2579673974
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085114del , CM000685.2:g.108085114del GRCh38
NC_000023.10:g.107328344del , CM000685.1:g.107328344del GRCh37
NC_000023.9:g.107215000del NCBI36
NG_012521.1:g.11505del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.541del MANE Select ENSP00000217958.3:p.Asp181MetfsTer?
ENST00000217958.7:c.541del ENSP00000217958.3:p.Asp181MetfsTer?
ENST00000340200.5:c.442del ENSP00000345963.5:p.Asp148MetfsTer?
ENST00000361815.9:c.*6del ENSP00000354906.5:n.*6del
ENST00000372295.5:c.418del ENSP00000361369.1:p.Asp140MetfsTer?
ENST00000372296.5:c.*6del ENSP00000361370.1:n.*6del
NM_002814.3:c.541del NP_002805.1:p.Asp181MetfsTer?
NM_170750.2:c.*6del NP_736606.1:n.*6del
NM_002814.4:c.541del MANE Select NP_002805.1:p.Asp181MetfsTer?
NM_170750.3:c.*6del NP_736606.1:n.*6del