Canonical Allele Identifier: CA2425838407

Gene: USP9X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41229319T= , CM000685.2:g.41229319T=	GRCh38
NC_000023.10:g.41088572T= , CM000685.1:g.41088572T=	GRCh37
NC_000023.9:g.40973516T=	NCBI36
NG_012547.1:g.148685T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7143T=	ENSP00000515603.1:p.Ser2381=
ENST00000703987.1:c.7143T=	ENSP00000515604.1:p.Ser2381=
ENST00000704649.1:c.3685-3068T=	ENSP00000515974.1:n.3685-3068T=
ENST00000704650.1:c.7128T=	ENSP00000515975.1:p.Ser2376=
ENST00000704651.1:c.6975T=	ENSP00000515976.1:p.Ser2325=
ENST00000704652.1:c.6227T=
ENST00000704654.1:c.4007T=
ENST00000704655.1:c.3271T=	ENSP00000515980.1:n.3271T=
ENST00000704656.1:c.2579T=	ENSP00000515981.1:n.2579T=
ENST00000324545.9:c.7128T=	ENSP00000316357.6:p.Ser2376=
ENST00000378308.7:c.7128T= MANE Select	ENSP00000367558.2:p.Ser2376=
ENST00000324545.8:c.7128T=	ENSP00000316357.6:p.Ser2376=
ENST00000378308.6:c.7128T=	ENSP00000367558.2:p.Ser2376=
ENST00000485180.1:n.337T=
NM_001039590.2:c.7128T=	NP_001034679.2:p.Ser2376=
NM_001039591.2:c.7128T=	NP_001034680.2:p.Ser2376=
XM_005272675.3:c.7143T=	XP_005272732.1:p.Ser2381=
XM_005272676.3:c.7143T=	XP_005272733.1:p.Ser2381=
XM_005272675.4:c.7143T=	XP_005272732.1:p.Ser2381=
XM_005272676.4:c.7143T=	XP_005272733.1:p.Ser2381=
NM_001039591.3:c.7128T= MANE Select	NP_001034680.2:p.Ser2376=
NM_001039590.3:c.7128T=	NP_001034679.2:p.Ser2376=