Canonical Allele Identifier: CA413841809
Gene: PSMD10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085121T>C , CM000685.2:g.108085121T>C GRCh38
NC_000023.10:g.107328351T>C , CM000685.1:g.107328351T>C GRCh37
NC_000023.9:g.107215007T>C NCBI36
NG_012521.1:g.11498A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.534A>G MANE Select ENSP00000217958.3:p.Leu178=
ENST00000217958.7:c.534A>G ENSP00000217958.3:p.Leu178=
ENST00000340200.5:c.435A>G ENSP00000345963.5:p.Leu145=
ENST00000361815.9:c.455A>G ENSP00000354906.5:p.Ter152Trp
ENST00000372295.5:c.411A>G ENSP00000361369.1:p.Leu137=
ENST00000372296.5:c.332A>G ENSP00000361370.1:p.Ter111Trp
NM_002814.3:c.534A>G NP_002805.1:p.Leu178=
NM_170750.2:c.455A>G NP_736606.1:p.Ter152Trp
NM_002814.4:c.534A>G MANE Select NP_002805.1:p.Leu178=
NM_170750.3:c.455A>G NP_736606.1:p.Ter152Trp