Canonical Allele Identifier: CA517921186

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328261G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085031G>T , CM000685.2:g.108085031G>T	GRCh38
NC_000023.10:g.107328261G>T , CM000685.1:g.107328261G>T	GRCh37
NC_000023.9:g.107214917G>T	NCBI36
NG_012521.1:g.11588C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.624C>A MANE Select	ENSP00000217958.3:p.Pro208=
ENST00000217958.7:c.624C>A	ENSP00000217958.3:p.Pro208=
ENST00000340200.5:c.525C>A	ENSP00000345963.5:p.Pro175=
ENST00000361815.9:c.*89C>A	ENSP00000354906.5:n.*89C>A
ENST00000372295.5:c.501C>A	ENSP00000361369.1:p.Pro167=
ENST00000372296.5:c.*89C>A	ENSP00000361370.1:n.*89C>A
NM_002814.3:c.624C>A	NP_002805.1:p.Pro208=
NM_170750.2:c.*89C>A	NP_736606.1:n.*89C>A
NM_002814.4:c.624C>A MANE Select	NP_002805.1:p.Pro208=
NM_170750.3:c.*89C>A	NP_736606.1:n.*89C>A