Canonical Allele Identifier: CA2450520157
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084450G= , CM000685.2:g.108084450G= GRCh38
NC_000023.10:g.107327680G= , CM000685.1:g.107327680G= GRCh37
NC_000023.9:g.107214336G= NCBI36
NG_012521.1:g.12169C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*524C= MANE Select ENSP00000217958.3:n.*524C=
ENST00000217958.7:c.*524C= ENSP00000217958.3:n.*524C=
NM_002814.3:c.*524C= NP_002805.1:n.*524C=
NM_170750.2:c.*670C= NP_736606.1:n.*670C=
NM_002814.4:c.*524C= MANE Select NP_002805.1:n.*524C=
NM_170750.3:c.*670C= NP_736606.1:n.*670C=