Canonical Allele Identifier: CA2450520305
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084946A= , CM000685.2:g.108084946A= GRCh38
NC_000023.10:g.107328176A= , CM000685.1:g.107328176A= GRCh37
NC_000023.9:g.107214832A= NCBI36
NG_012521.1:g.11673T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*28T= MANE Select ENSP00000217958.3:n.*28T=
ENST00000217958.7:c.*28T= ENSP00000217958.3:n.*28T=
ENST00000340200.5:c.610T= ENSP00000345963.5:n.610T=
ENST00000361815.9:c.*174T= ENSP00000354906.5:n.*174T=
ENST00000372295.5:c.*28T= ENSP00000361369.1:n.*28T=
ENST00000372296.5:c.*174T= ENSP00000361370.1:n.*174T=
NM_002814.3:c.*28T= NP_002805.1:n.*28T=
NM_170750.2:c.*174T= NP_736606.1:n.*174T=
NM_002814.4:c.*28T= MANE Select NP_002805.1:n.*28T=
NM_170750.3:c.*174T= NP_736606.1:n.*174T=