Canonical Allele Identifier: CA1136170158
Gene: PSMD10 HGNC NCBI

Linked Data

dbSNP Id: rs2031475266

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084701G>A , CM000685.2:g.108084701G>A GRCh38
NC_000023.10:g.107327931G>A , CM000685.1:g.107327931G>A GRCh37
NC_000023.9:g.107214587G>A NCBI36
NG_012521.1:g.11918C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*273C>T MANE Select ENSP00000217958.3:n.*273C>T
ENST00000217958.7:c.*273C>T ENSP00000217958.3:n.*273C>T
ENST00000372296.5:c.*419C>T ENSP00000361370.1:n.*419C>T
NM_002814.3:c.*273C>T NP_002805.1:n.*273C>T
NM_170750.2:c.*419C>T NP_736606.1:n.*419C>T
NM_002814.4:c.*273C>T MANE Select NP_002805.1:n.*273C>T
NM_170750.3:c.*419C>T NP_736606.1:n.*419C>T