Canonical Allele Identifier: CA517921205

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328297T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085067T>C , CM000685.2:g.108085067T>C	GRCh38
NC_000023.10:g.107328297T>C , CM000685.1:g.107328297T>C	GRCh37
NC_000023.9:g.107214953T>C	NCBI36
NG_012521.1:g.11552A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.588A>G MANE Select	ENSP00000217958.3:p.Ala196=
ENST00000217958.7:c.588A>G	ENSP00000217958.3:p.Ala196=
ENST00000340200.5:c.489A>G	ENSP00000345963.5:p.Ala163=
ENST00000361815.9:c.*53A>G	ENSP00000354906.5:n.*53A>G
ENST00000372295.5:c.465A>G	ENSP00000361369.1:p.Ala155=
ENST00000372296.5:c.*53A>G	ENSP00000361370.1:n.*53A>G
NM_002814.3:c.588A>G	NP_002805.1:p.Ala196=
NM_170750.2:c.*53A>G	NP_736606.1:n.*53A>G
NM_002814.4:c.588A>G MANE Select	NP_002805.1:p.Ala196=
NM_170750.3:c.*53A>G	NP_736606.1:n.*53A>G