Canonical Allele Identifier: CA517921201

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328291A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085061A>G , CM000685.2:g.108085061A>G	GRCh38
NC_000023.10:g.107328291A>G , CM000685.1:g.107328291A>G	GRCh37
NC_000023.9:g.107214947A>G	NCBI36
NG_012521.1:g.11558T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.594T>C MANE Select	ENSP00000217958.3:p.Ile198=
ENST00000217958.7:c.594T>C	ENSP00000217958.3:p.Ile198=
ENST00000340200.5:c.495T>C	ENSP00000345963.5:p.Ile165=
ENST00000361815.9:c.*59T>C	ENSP00000354906.5:n.*59T>C
ENST00000372295.5:c.471T>C	ENSP00000361369.1:p.Ile157=
ENST00000372296.5:c.*59T>C	ENSP00000361370.1:n.*59T>C
NM_002814.3:c.594T>C	NP_002805.1:p.Ile198=
NM_170750.2:c.*59T>C	NP_736606.1:n.*59T>C
NM_002814.4:c.594T>C MANE Select	NP_002805.1:p.Ile198=
NM_170750.3:c.*59T>C	NP_736606.1:n.*59T>C