Canonical Allele Identifier: CA517921216

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328312C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085082C>G , CM000685.2:g.108085082C>G	GRCh38
NC_000023.10:g.107328312C>G , CM000685.1:g.107328312C>G	GRCh37
NC_000023.9:g.107214968C>G	NCBI36
NG_012521.1:g.11537G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.573G>C MANE Select	ENSP00000217958.3:p.Leu191=
ENST00000217958.7:c.573G>C	ENSP00000217958.3:p.Leu191=
ENST00000340200.5:c.474G>C	ENSP00000345963.5:p.Leu158=
ENST00000361815.9:c.*38G>C	ENSP00000354906.5:n.*38G>C
ENST00000372295.5:c.450G>C	ENSP00000361369.1:p.Leu150=
ENST00000372296.5:c.*38G>C	ENSP00000361370.1:n.*38G>C
NM_002814.3:c.573G>C	NP_002805.1:p.Leu191=
NM_170750.2:c.*38G>C	NP_736606.1:n.*38G>C
NM_002814.4:c.573G>C MANE Select	NP_002805.1:p.Leu191=
NM_170750.3:c.*38G>C	NP_736606.1:n.*38G>C