Canonical Allele Identifier: CA516347846

Gene: USP9X

Linked Data

• MyVariant Identifiers: chrX:g.41088641T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41229388T>G , CM000685.2:g.41229388T>G	GRCh38
NC_000023.10:g.41088641T>G , CM000685.1:g.41088641T>G	GRCh37
NC_000023.9:g.40973585T>G	NCBI36
NG_012547.1:g.148754T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7212T>G	ENSP00000515603.1:p.Pro2404=
ENST00000703987.1:c.7212T>G	ENSP00000515604.1:p.Pro2404=
ENST00000704649.1:c.3685-2999T>G	ENSP00000515974.1:n.3685-2999T>G
ENST00000704650.1:c.7197T>G	ENSP00000515975.1:p.Pro2399=
ENST00000704651.1:c.7044T>G	ENSP00000515976.1:p.Pro2348=
ENST00000704652.1:c.6296T>G
ENST00000704654.1:c.4076T>G
ENST00000704655.1:c.3340T>G	ENSP00000515980.1:n.3340T>G
ENST00000704656.1:c.2648T>G	ENSP00000515981.1:n.2648T>G
ENST00000324545.9:c.7197T>G	ENSP00000316357.6:p.Pro2399=
ENST00000378308.7:c.7197T>G MANE Select	ENSP00000367558.2:p.Pro2399=
ENST00000324545.8:c.7197T>G	ENSP00000316357.6:p.Pro2399=
ENST00000378308.6:c.7197T>G	ENSP00000367558.2:p.Pro2399=
ENST00000485180.1:n.406T>G
NM_001039590.2:c.7197T>G	NP_001034679.2:p.Pro2399=
NM_001039591.2:c.7197T>G	NP_001034680.2:p.Pro2399=
XM_005272675.3:c.7212T>G	XP_005272732.1:p.Pro2404=
XM_005272676.3:c.7212T>G	XP_005272733.1:p.Pro2404=
XM_005272675.4:c.7212T>G	XP_005272732.1:p.Pro2404=
XM_005272676.4:c.7212T>G	XP_005272733.1:p.Pro2404=
NM_001039591.3:c.7197T>G MANE Select	NP_001034680.2:p.Pro2399=
NM_001039590.3:c.7197T>G	NP_001034679.2:p.Pro2399=