Canonical Allele Identifier: CA2425838745

Gene: USP9X

Linked Data

• dbSNP Id: rs2063350701

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41230420_41230421insG , CM000685.2:g.41230420_41230421insG	GRCh38
NC_000023.10:g.41089673_41089674insG , CM000685.1:g.41089673_41089674insG	GRCh37
NC_000023.9:g.40974617_40974618insG	NCBI36
NG_012547.1:g.149786_149787insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7447-81_7447-80insG	ENSP00000515603.1:n.7447-81_7447-80insG
ENST00000703987.1:c.7495-81_7495-80insG	ENSP00000515604.1:n.7495-81_7495-80insG
ENST00000704649.1:c.3685-1967_3685-1966insG	ENSP00000515974.1:n.3685-1967_3685-1966insG
ENST00000704650.1:c.7432-81_7432-80insG	ENSP00000515975.1:n.7432-81_7432-80insG
ENST00000704651.1:c.7279-81_7279-80insG	ENSP00000515976.1:n.7279-81_7279-80insG
ENST00000704652.1:c.6531-81_6531-80insG
ENST00000704654.1:c.4311-81_4311-80insG
ENST00000704655.1:c.3575-81_3575-80insG	ENSP00000515980.1:n.3575-81_3575-80insG
ENST00000704656.1:c.2883-81_2883-80insG	ENSP00000515981.1:n.2883-81_2883-80insG
ENST00000324545.9:c.7480-81_7480-80insG	ENSP00000316357.6:n.7480-81_7480-80insG
ENST00000378308.7:c.7432-81_7432-80insG MANE Select	ENSP00000367558.2:n.7432-81_7432-80insG
ENST00000324545.8:c.7480-81_7480-80insG	ENSP00000316357.6:n.7480-81_7480-80insG
ENST00000378308.6:c.7432-81_7432-80insG	ENSP00000367558.2:n.7432-81_7432-80insG
NM_001039590.2:c.7480-81_7480-80insG	NP_001034679.2:n.7480-81_7480-80insG
NM_001039591.2:c.7432-81_7432-80insG	NP_001034680.2:n.7432-81_7432-80insG
XM_005272675.3:c.7495-81_7495-80insG	XP_005272732.1:n.7495-81_7495-80insG
XM_005272676.3:c.7447-81_7447-80insG	XP_005272733.1:n.7447-81_7447-80insG
XM_005272675.4:c.7495-81_7495-80insG	XP_005272732.1:n.7495-81_7495-80insG
XM_005272676.4:c.7447-81_7447-80insG	XP_005272733.1:n.7447-81_7447-80insG
NM_001039591.3:c.7432-81_7432-80insG MANE Select	NP_001034680.2:n.7432-81_7432-80insG
NM_001039590.3:c.7480-81_7480-80insG	NP_001034679.2:n.7480-81_7480-80insG