Canonical Allele Identifier: CA2514615170
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084874C>A , CM000685.2:g.108084874C>A GRCh38
NC_000023.10:g.107328104C>A , CM000685.1:g.107328104C>A GRCh37
NC_000023.9:g.107214760C>A NCBI36
NG_012521.1:g.11745G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000217958.8:c.*100G>T MANE Select ENSP00000217958.3:n.*100G>T
ENST00000217958.7:c.*100G>T ENSP00000217958.3:n.*100G>T
ENST00000340200.5:c.682G>T ENSP00000345963.5:n.682G>T
ENST00000361815.9:c.*246G>T ENSP00000354906.5:n.*246G>T
ENST00000372295.5:c.*100G>T ENSP00000361369.1:n.*100G>T
ENST00000372296.5:c.*246G>T ENSP00000361370.1:n.*246G>T
NM_002814.3:c.*100G>T NP_002805.1:n.*100G>T
NM_170750.2:c.*246G>T NP_736606.1:n.*246G>T
NM_002814.4:c.*100G>T MANE Select NP_002805.1:n.*100G>T
NM_170750.3:c.*246G>T NP_736606.1:n.*246G>T