Canonical Allele Identifier: CA413841802

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328349G>A (hg19) ; chrX:g.108085119G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085119G>A , CM000685.2:g.108085119G>A	GRCh38
NC_000023.10:g.107328349G>A , CM000685.1:g.107328349G>A	GRCh37
NC_000023.9:g.107215005G>A	NCBI36
NG_012521.1:g.11500C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.536C>T MANE Select	ENSP00000217958.3:p.Ala179Val
ENST00000217958.7:c.536C>T	ENSP00000217958.3:p.Ala179Val
ENST00000340200.5:c.437C>T	ENSP00000345963.5:p.Ala146Val
ENST00000361815.9:c.*1C>T	ENSP00000354906.5:n.*1C>T
ENST00000372295.5:c.413C>T	ENSP00000361369.1:p.Ala138Val
ENST00000372296.5:c.*1C>T	ENSP00000361370.1:n.*1C>T
NM_002814.3:c.536C>T	NP_002805.1:p.Ala179Val
NM_170750.2:c.*1C>T	NP_736606.1:n.*1C>T
NM_002814.4:c.536C>T MANE Select	NP_002805.1:p.Ala179Val
NM_170750.3:c.*1C>T	NP_736606.1:n.*1C>T