Canonical Allele Identifier: CA2450520340
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085116C= , CM000685.2:g.108085116C= GRCh38
NC_000023.10:g.107328346C= , CM000685.1:g.107328346C= GRCh37
NC_000023.9:g.107215002C= NCBI36
NG_012521.1:g.11503G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.539G= MANE Select ENSP00000217958.3:p.Cys180=
ENST00000217958.7:c.539G= ENSP00000217958.3:p.Cys180=
ENST00000340200.5:c.440G= ENSP00000345963.5:p.Cys147=
ENST00000361815.9:c.*4G= ENSP00000354906.5:n.*4G=
ENST00000372295.5:c.416G= ENSP00000361369.1:p.Cys139=
ENST00000372296.5:c.*4G= ENSP00000361370.1:n.*4G=
NM_002814.3:c.539G= NP_002805.1:p.Cys180=
NM_170750.2:c.*4G= NP_736606.1:n.*4G=
NM_002814.4:c.539G= MANE Select NP_002805.1:p.Cys180=
NM_170750.3:c.*4G= NP_736606.1:n.*4G=