Canonical Allele Identifier: CA517921208

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328300T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085070T>G , CM000685.2:g.108085070T>G	GRCh38
NC_000023.10:g.107328300T>G , CM000685.1:g.107328300T>G	GRCh37
NC_000023.9:g.107214956T>G	NCBI36
NG_012521.1:g.11549A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.585A>C MANE Select	ENSP00000217958.3:p.Gly195=
ENST00000217958.7:c.585A>C	ENSP00000217958.3:p.Gly195=
ENST00000340200.5:c.486A>C	ENSP00000345963.5:p.Gly162=
ENST00000361815.9:c.*50A>C	ENSP00000354906.5:n.*50A>C
ENST00000372295.5:c.462A>C	ENSP00000361369.1:p.Gly154=
ENST00000372296.5:c.*50A>C	ENSP00000361370.1:n.*50A>C
NM_002814.3:c.585A>C	NP_002805.1:p.Gly195=
NM_170750.2:c.*50A>C	NP_736606.1:n.*50A>C
NM_002814.4:c.585A>C MANE Select	NP_002805.1:p.Gly195=
NM_170750.3:c.*50A>C	NP_736606.1:n.*50A>C