Canonical Allele Identifier: CA2694424138
Gene: PSMD10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084656del , CM000685.2:g.108084656del GRCh38
NC_000023.10:g.107327886del , CM000685.1:g.107327886del GRCh37
NC_000023.9:g.107214542del NCBI36
NG_012521.1:g.11963del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*318del MANE Select ENSP00000217958.3:n.*318del
ENST00000217958.7:c.*318del ENSP00000217958.3:n.*318del
ENST00000372296.5:c.*464del ENSP00000361370.1:n.*464del
NM_002814.3:c.*318del NP_002805.1:n.*318del
NM_170750.2:c.*464del NP_736606.1:n.*464del
NM_002814.4:c.*318del MANE Select NP_002805.1:n.*318del
NM_170750.3:c.*464del NP_736606.1:n.*464del