Canonical Allele Identifier: CA413841776

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328338C>A (hg19) ; chrX:g.108085108C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085108C>A , CM000685.2:g.108085108C>A	GRCh38
NC_000023.10:g.107328338C>A , CM000685.1:g.107328338C>A	GRCh37
NC_000023.9:g.107214994C>A	NCBI36
NG_012521.1:g.11511G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.547G>T MANE Select	ENSP00000217958.3:p.Glu183Ter
ENST00000217958.7:c.547G>T	ENSP00000217958.3:p.Glu183Ter
ENST00000340200.5:c.448G>T	ENSP00000345963.5:p.Glu150Ter
ENST00000361815.9:c.*12G>T	ENSP00000354906.5:n.*12G>T
ENST00000372295.5:c.424G>T	ENSP00000361369.1:p.Glu142Ter
ENST00000372296.5:c.*12G>T	ENSP00000361370.1:n.*12G>T
NM_002814.3:c.547G>T	NP_002805.1:p.Glu183Ter
NM_170750.2:c.*12G>T	NP_736606.1:n.*12G>T
NM_002814.4:c.547G>T MANE Select	NP_002805.1:p.Glu183Ter
NM_170750.3:c.*12G>T	NP_736606.1:n.*12G>T