Canonical Allele Identifier: CA2531325960
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084948dup , CM000685.2:g.108084948dup GRCh38
NC_000023.10:g.107328178dup , CM000685.1:g.107328178dup GRCh37
NC_000023.9:g.107214834dup NCBI36
NG_012521.1:g.11671dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*26dup MANE Select ENSP00000217958.3:n.*26dup
ENST00000217958.7:c.*26dup ENSP00000217958.3:n.*26dup
ENST00000340200.5:c.608dup ENSP00000345963.5:n.608dup
ENST00000361815.9:c.*172dup ENSP00000354906.5:n.*172dup
ENST00000372295.5:c.*26dup ENSP00000361369.1:n.*26dup
ENST00000372296.5:c.*172dup ENSP00000361370.1:n.*172dup
NM_002814.3:c.*26dup NP_002805.1:n.*26dup
NM_170750.2:c.*172dup NP_736606.1:n.*172dup
NM_002814.4:c.*26dup MANE Select NP_002805.1:n.*26dup
NM_170750.3:c.*172dup NP_736606.1:n.*172dup