Canonical Allele Identifier: CA2450520320
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085009G= , CM000685.2:g.108085009G= GRCh38
NC_000023.10:g.107328239G= , CM000685.1:g.107328239G= GRCh37
NC_000023.9:g.107214895G= NCBI36
NG_012521.1:g.11610C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.646C= MANE Select ENSP00000217958.3:p.Leu216=
ENST00000217958.7:c.646C= ENSP00000217958.3:p.Leu216=
ENST00000340200.5:c.547C= ENSP00000345963.5:p.Leu183=
ENST00000361815.9:c.*111C= ENSP00000354906.5:n.*111C=
ENST00000372295.5:c.523C= ENSP00000361369.1:p.Leu175=
ENST00000372296.5:c.*111C= ENSP00000361370.1:n.*111C=
NM_002814.3:c.646C= NP_002805.1:p.Leu216=
NM_170750.2:c.*111C= NP_736606.1:n.*111C=
NM_002814.4:c.646C= MANE Select NP_002805.1:p.Leu216=
NM_170750.3:c.*111C= NP_736606.1:n.*111C=