Canonical Allele Identifier: CA2450520257
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084787T= , CM000685.2:g.108084787T= GRCh38
NC_000023.10:g.107328017T= , CM000685.1:g.107328017T= GRCh37
NC_000023.9:g.107214673T= NCBI36
NG_012521.1:g.11832A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*187A= MANE Select ENSP00000217958.3:n.*187A=
ENST00000217958.7:c.*187A= ENSP00000217958.3:n.*187A=
ENST00000372295.5:c.*187A= ENSP00000361369.1:n.*187A=
ENST00000372296.5:c.*333A= ENSP00000361370.1:n.*333A=
NM_002814.3:c.*187A= NP_002805.1:n.*187A=
NM_170750.2:c.*333A= NP_736606.1:n.*333A=
NM_002814.4:c.*187A= MANE Select NP_002805.1:n.*187A=
NM_170750.3:c.*333A= NP_736606.1:n.*333A=