Canonical Allele Identifier: CA413841819

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328355T>G (hg19) ; chrX:g.108085125T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085125T>G , CM000685.2:g.108085125T>G	GRCh38
NC_000023.10:g.107328355T>G , CM000685.1:g.107328355T>G	GRCh37
NC_000023.9:g.107215011T>G	NCBI36
NG_012521.1:g.11494A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.530A>C MANE Select	ENSP00000217958.3:p.His177Pro
ENST00000217958.7:c.530A>C	ENSP00000217958.3:p.His177Pro
ENST00000340200.5:c.431A>C	ENSP00000345963.5:p.His144Pro
ENST00000361815.9:c.451A>C	ENSP00000354906.5:p.Thr151Pro
ENST00000372295.5:c.407A>C	ENSP00000361369.1:p.His136Pro
ENST00000372296.5:c.328A>C	ENSP00000361370.1:p.Thr110Pro
NM_002814.3:c.530A>C	NP_002805.1:p.His177Pro
NM_170750.2:c.451A>C	NP_736606.1:p.Thr151Pro
NM_002814.4:c.530A>C MANE Select	NP_002805.1:p.His177Pro
NM_170750.3:c.451A>C	NP_736606.1:p.Thr151Pro