Canonical Allele Identifier: CA412751986

Gene: USP9X

Linked Data

• MyVariant Identifiers: chrX:g.41088559C>G (hg19) ; chrX:g.41229306C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41229306C>G , CM000685.2:g.41229306C>G	GRCh38
NC_000023.10:g.41088559C>G , CM000685.1:g.41088559C>G	GRCh37
NC_000023.9:g.40973503C>G	NCBI36
NG_012547.1:g.148672C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000703986.1:c.7130C>G	ENSP00000515603.1:p.Thr2377Arg
ENST00000703987.1:c.7130C>G	ENSP00000515604.1:p.Thr2377Arg
ENST00000704649.1:c.3685-3081C>G	ENSP00000515974.1:n.3685-3081C>G
ENST00000704650.1:c.7115C>G	ENSP00000515975.1:p.Thr2372Arg
ENST00000704651.1:c.6962C>G	ENSP00000515976.1:p.Thr2321Arg
ENST00000704652.1:c.6214C>G
ENST00000704654.1:c.3994C>G
ENST00000704655.1:c.3258C>G	ENSP00000515980.1:n.3258C>G
ENST00000704656.1:c.2566C>G	ENSP00000515981.1:n.2566C>G
ENST00000324545.9:c.7115C>G	ENSP00000316357.6:p.Thr2372Arg
ENST00000378308.7:c.7115C>G MANE Select	ENSP00000367558.2:p.Thr2372Arg
ENST00000324545.8:c.7115C>G	ENSP00000316357.6:p.Thr2372Arg
ENST00000378308.6:c.7115C>G	ENSP00000367558.2:p.Thr2372Arg
ENST00000485180.1:n.324C>G
NM_001039590.2:c.7115C>G	NP_001034679.2:p.Thr2372Arg
NM_001039591.2:c.7115C>G	NP_001034680.2:p.Thr2372Arg
XM_005272675.3:c.7130C>G	XP_005272732.1:p.Thr2377Arg
XM_005272676.3:c.7130C>G	XP_005272733.1:p.Thr2377Arg
XM_005272675.4:c.7130C>G	XP_005272732.1:p.Thr2377Arg
XM_005272676.4:c.7130C>G	XP_005272733.1:p.Thr2377Arg
NM_001039591.3:c.7115C>G MANE Select	NP_001034680.2:p.Thr2372Arg
NM_001039590.3:c.7115C>G	NP_001034679.2:p.Thr2372Arg