Canonical Allele Identifier: CA2450520266
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084812C= , CM000685.2:g.108084812C= GRCh38
NC_000023.10:g.107328042C= , CM000685.1:g.107328042C= GRCh37
NC_000023.9:g.107214698C= NCBI36
NG_012521.1:g.11807G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*162G= MANE Select ENSP00000217958.3:n.*162G=
ENST00000217958.7:c.*162G= ENSP00000217958.3:n.*162G=
ENST00000372295.5:c.*162G= ENSP00000361369.1:n.*162G=
ENST00000372296.5:c.*308G= ENSP00000361370.1:n.*308G=
NM_002814.3:c.*162G= NP_002805.1:n.*162G=
NM_170750.2:c.*308G= NP_736606.1:n.*308G=
NM_002814.4:c.*162G= MANE Select NP_002805.1:n.*162G=
NM_170750.3:c.*308G= NP_736606.1:n.*308G=