Canonical Allele Identifier: CA2694424151
Gene: PSMD10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084677G>A , CM000685.2:g.108084677G>A GRCh38
NC_000023.10:g.107327907G>A , CM000685.1:g.107327907G>A GRCh37
NC_000023.9:g.107214563G>A NCBI36
NG_012521.1:g.11942C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*297C>T MANE Select ENSP00000217958.3:n.*297C>T
ENST00000217958.7:c.*297C>T ENSP00000217958.3:n.*297C>T
ENST00000372296.5:c.*443C>T ENSP00000361370.1:n.*443C>T
NM_002814.3:c.*297C>T NP_002805.1:n.*297C>T
NM_170750.2:c.*443C>T NP_736606.1:n.*443C>T
NM_002814.4:c.*297C>T MANE Select NP_002805.1:n.*297C>T
NM_170750.3:c.*443C>T NP_736606.1:n.*443C>T