Canonical Allele Identifier: CA2450520208
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084623C= , CM000685.2:g.108084623C= GRCh38
NC_000023.10:g.107327853C= , CM000685.1:g.107327853C= GRCh37
NC_000023.9:g.107214509C= NCBI36
NG_012521.1:g.11996G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*351G= MANE Select ENSP00000217958.3:n.*351G=
ENST00000217958.7:c.*351G= ENSP00000217958.3:n.*351G=
ENST00000372296.5:c.*497G= ENSP00000361370.1:n.*497G=
NM_002814.3:c.*351G= NP_002805.1:n.*351G=
NM_170750.2:c.*497G= NP_736606.1:n.*497G=
NM_002814.4:c.*351G= MANE Select NP_002805.1:n.*351G=
NM_170750.3:c.*497G= NP_736606.1:n.*497G=