Canonical Allele Identifier: CA2514253728
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084910C>A , CM000685.2:g.108084910C>A GRCh38
NC_000023.10:g.107328140C>A , CM000685.1:g.107328140C>A GRCh37
NC_000023.9:g.107214796C>A NCBI36
NG_012521.1:g.11709G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*64G>T MANE Select ENSP00000217958.3:n.*64G>T
ENST00000217958.7:c.*64G>T ENSP00000217958.3:n.*64G>T
ENST00000340200.5:c.646G>T ENSP00000345963.5:n.646G>T
ENST00000361815.9:c.*210G>T ENSP00000354906.5:n.*210G>T
ENST00000372295.5:c.*64G>T ENSP00000361369.1:n.*64G>T
ENST00000372296.5:c.*210G>T ENSP00000361370.1:n.*210G>T
NM_002814.3:c.*64G>T NP_002805.1:n.*64G>T
NM_170750.2:c.*210G>T NP_736606.1:n.*210G>T
NM_002814.4:c.*64G>T MANE Select NP_002805.1:n.*64G>T
NM_170750.3:c.*210G>T NP_736606.1:n.*210G>T