Canonical Allele Identifier: CA413841752

Gene: PSMD10

Linked Data

• COSMIC: COSM404529
• MyVariant Identifiers: chrX:g.107328328T>G (hg19) ; chrX:g.108085098T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085098T>G , CM000685.2:g.108085098T>G	GRCh38
NC_000023.10:g.107328328T>G , CM000685.1:g.107328328T>G	GRCh37
NC_000023.9:g.107214984T>G	NCBI36
NG_012521.1:g.11521A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.557A>C MANE Select	ENSP00000217958.3:p.Glu186Ala
ENST00000217958.7:c.557A>C	ENSP00000217958.3:p.Glu186Ala
ENST00000340200.5:c.458A>C	ENSP00000345963.5:p.Glu153Ala
ENST00000361815.9:c.*22A>C	ENSP00000354906.5:n.*22A>C
ENST00000372295.5:c.434A>C	ENSP00000361369.1:p.Glu145Ala
ENST00000372296.5:c.*22A>C	ENSP00000361370.1:n.*22A>C
NM_002814.3:c.557A>C	NP_002805.1:p.Glu186Ala
NM_170750.2:c.*22A>C	NP_736606.1:n.*22A>C
NM_002814.4:c.557A>C MANE Select	NP_002805.1:p.Glu186Ala
NM_170750.3:c.*22A>C	NP_736606.1:n.*22A>C