Canonical Allele Identifier: CA333053199

Gene: PSMD10

Linked Data

• dbSNP Id: rs369453085
• MyVariant Identifiers: chrX:g.107327579T>A (hg19) ; chrX:g.108084349T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084349T>A , CM000685.2:g.108084349T>A	GRCh38
NC_000023.10:g.107327579T>A , CM000685.1:g.107327579T>A	GRCh37
NC_000023.9:g.107214235T>A	NCBI36
NG_012521.1:g.12270A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*625A>T MANE Select	ENSP00000217958.3:n.*625A>T
ENST00000217958.7:c.*625A>T	ENSP00000217958.3:n.*625A>T
NM_002814.3:c.*625A>T	NP_002805.1:n.*625A>T
NM_170750.2:c.*771A>T	NP_736606.1:n.*771A>T
NM_002814.4:c.*625A>T MANE Select	NP_002805.1:n.*625A>T
NM_170750.3:c.*771A>T	NP_736606.1:n.*771A>T