Canonical Allele Identifier: CA2450520264
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084805T= , CM000685.2:g.108084805T= GRCh38
NC_000023.10:g.107328035T= , CM000685.1:g.107328035T= GRCh37
NC_000023.9:g.107214691T= NCBI36
NG_012521.1:g.11814A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*169A= MANE Select ENSP00000217958.3:n.*169A=
ENST00000217958.7:c.*169A= ENSP00000217958.3:n.*169A=
ENST00000372295.5:c.*169A= ENSP00000361369.1:n.*169A=
ENST00000372296.5:c.*315A= ENSP00000361370.1:n.*315A=
NM_002814.3:c.*169A= NP_002805.1:n.*169A=
NM_170750.2:c.*315A= NP_736606.1:n.*315A=
NM_002814.4:c.*169A= MANE Select NP_002805.1:n.*169A=
NM_170750.3:c.*315A= NP_736606.1:n.*315A=