Canonical Allele Identifier: CA2450520227
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084693_108084695delinsTCA , CM000685.2:g.108084693_108084695delinsTCA GRCh38
NC_000023.10:g.107327923_107327925delinsTCA , CM000685.1:g.107327923_107327925delinsTCA GRCh37
NC_000023.9:g.107214579_107214581delinsTCA NCBI36
NG_012521.1:g.11924_11926delinsTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*279_*281delinsTGA MANE Select ENSP00000217958.3:n.*279_*281delinsTGA
ENST00000217958.7:c.*279_*281delinsTGA ENSP00000217958.3:n.*279_*281delinsTGA
ENST00000372296.5:c.*425_*427delinsTGA ENSP00000361370.1:n.*425_*427delinsTGA
NM_002814.3:c.*279_*281delinsTGA NP_002805.1:n.*279_*281delinsTGA
NM_170750.2:c.*425_*427delinsTGA NP_736606.1:n.*425_*427delinsTGA
NM_002814.4:c.*279_*281delinsTGA MANE Select NP_002805.1:n.*279_*281delinsTGA
NM_170750.3:c.*425_*427delinsTGA NP_736606.1:n.*425_*427delinsTGA