Canonical Allele Identifier: CA412754329

Gene: USP9X

Linked Data

• MyVariant Identifiers: chrX:g.41089757C>A (hg19) ; chrX:g.41230504C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41230504C>A , CM000685.2:g.41230504C>A	GRCh38
NC_000023.10:g.41089757C>A , CM000685.1:g.41089757C>A	GRCh37
NC_000023.9:g.40974701C>A	NCBI36
NG_012547.1:g.149870C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7450C>A	ENSP00000515603.1:p.Pro2484Thr
ENST00000703987.1:c.7498C>A	ENSP00000515604.1:p.Pro2500Thr
ENST00000704649.1:c.3685-1883C>A	ENSP00000515974.1:n.3685-1883C>A
ENST00000704650.1:c.7435C>A	ENSP00000515975.1:p.Pro2479Thr
ENST00000704651.1:c.7282C>A	ENSP00000515976.1:p.Pro2428Thr
ENST00000704652.1:c.6534C>A
ENST00000704654.1:c.4314C>A
ENST00000704655.1:c.3578C>A	ENSP00000515980.1:n.3578C>A
ENST00000704656.1:c.2886C>A	ENSP00000515981.1:n.2886C>A
ENST00000324545.9:c.7483C>A	ENSP00000316357.6:p.Pro2495Thr
ENST00000378308.7:c.7435C>A MANE Select	ENSP00000367558.2:p.Pro2479Thr
ENST00000324545.8:c.7483C>A	ENSP00000316357.6:p.Pro2495Thr
ENST00000378308.6:c.7435C>A	ENSP00000367558.2:p.Pro2479Thr
NM_001039590.2:c.7483C>A	NP_001034679.2:p.Pro2495Thr
NM_001039591.2:c.7435C>A	NP_001034680.2:p.Pro2479Thr
XM_005272675.3:c.7498C>A	XP_005272732.1:p.Pro2500Thr
XM_005272676.3:c.7450C>A	XP_005272733.1:p.Pro2484Thr
XM_005272675.4:c.7498C>A	XP_005272732.1:p.Pro2500Thr
XM_005272676.4:c.7450C>A	XP_005272733.1:p.Pro2484Thr
NM_001039591.3:c.7435C>A MANE Select	NP_001034680.2:p.Pro2479Thr
NM_001039590.3:c.7483C>A	NP_001034679.2:p.Pro2495Thr