Canonical Allele Identifier: CA2450520229
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084698A= , CM000685.2:g.108084698A= GRCh38
NC_000023.10:g.107327928A= , CM000685.1:g.107327928A= GRCh37
NC_000023.9:g.107214584A= NCBI36
NG_012521.1:g.11921T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*276T= MANE Select ENSP00000217958.3:n.*276T=
ENST00000217958.7:c.*276T= ENSP00000217958.3:n.*276T=
ENST00000372296.5:c.*422T= ENSP00000361370.1:n.*422T=
NM_002814.3:c.*276T= NP_002805.1:n.*276T=
NM_170750.2:c.*422T= NP_736606.1:n.*422T=
NM_002814.4:c.*276T= MANE Select NP_002805.1:n.*276T=
NM_170750.3:c.*422T= NP_736606.1:n.*422T=