Canonical Allele Identifier: CA10389238

Gene: USP9X

Linked Data

• dbSNP Id: rs759238531
• ExAC: X:41089872 T / A
• gnomAD v2: X-41089872-T-A
• gnomAD v4: X-41230619-T-A
• MyVariant Identifiers: chrX:g.41089872T>A (hg19) ; chrX:g.41230619T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41230619T>A , CM000685.2:g.41230619T>A	GRCh38
NC_000023.10:g.41089872T>A , CM000685.1:g.41089872T>A	GRCh37
NC_000023.9:g.40974816T>A	NCBI36
NG_012547.1:g.149985T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7542+23T>A	ENSP00000515603.1:n.7542+23T>A
ENST00000703987.1:c.7590+23T>A	ENSP00000515604.1:n.7590+23T>A
ENST00000704649.1:c.3685-1768T>A	ENSP00000515974.1:n.3685-1768T>A
ENST00000704650.1:c.7527+23T>A	ENSP00000515975.1:n.7527+23T>A
ENST00000704651.1:c.7374+23T>A	ENSP00000515976.1:n.7374+23T>A
ENST00000704652.1:c.6626+23T>A
ENST00000704654.1:c.4406+23T>A
ENST00000704655.1:c.3670+23T>A	ENSP00000515980.1:n.3670+23T>A
ENST00000704656.1:c.2978+23T>A	ENSP00000515981.1:n.2978+23T>A
ENST00000324545.9:c.7575+23T>A	ENSP00000316357.6:n.7575+23T>A
ENST00000378308.7:c.7527+23T>A MANE Select	ENSP00000367558.2:n.7527+23T>A
ENST00000324545.8:c.7575+23T>A	ENSP00000316357.6:n.7575+23T>A
ENST00000378308.6:c.7527+23T>A	ENSP00000367558.2:n.7527+23T>A
NM_001039590.2:c.7575+23T>A	NP_001034679.2:n.7575+23T>A
NM_001039591.2:c.7527+23T>A	NP_001034680.2:n.7527+23T>A
XM_005272675.3:c.7590+23T>A	XP_005272732.1:n.7590+23T>A
XM_005272676.3:c.7542+23T>A	XP_005272733.1:n.7542+23T>A
XM_005272675.4:c.7590+23T>A	XP_005272732.1:n.7590+23T>A
XM_005272676.4:c.7542+23T>A	XP_005272733.1:n.7542+23T>A
NM_001039591.3:c.7527+23T>A MANE Select	NP_001034680.2:n.7527+23T>A
NM_001039590.3:c.7575+23T>A	NP_001034679.2:n.7575+23T>A