Canonical Allele Identifier: CA1136170191
Gene: PSMD10 HGNC NCBI

Linked Data

dbSNP Id: rs2031476034

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084764G>A , CM000685.2:g.108084764G>A GRCh38
NC_000023.10:g.107327994G>A , CM000685.1:g.107327994G>A GRCh37
NC_000023.9:g.107214650G>A NCBI36
NG_012521.1:g.11855C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*210C>T MANE Select ENSP00000217958.3:n.*210C>T
ENST00000217958.7:c.*210C>T ENSP00000217958.3:n.*210C>T
ENST00000372296.5:c.*356C>T ENSP00000361370.1:n.*356C>T
NM_002814.3:c.*210C>T NP_002805.1:n.*210C>T
NM_170750.2:c.*356C>T NP_736606.1:n.*356C>T
NM_002814.4:c.*210C>T MANE Select NP_002805.1:n.*210C>T
NM_170750.3:c.*356C>T NP_736606.1:n.*356C>T