Canonical Allele Identifier: CA2425806583

Gene: USP9X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41136805G= , CM000685.2:g.41136805G=	GRCh38
NC_000023.10:g.40996058G= , CM000685.1:g.40996058G=	GRCh37
NC_000023.9:g.40881002G=	NCBI36
NG_012547.1:g.56171G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000703986.1:c.437G=	ENSP00000515603.1:p.Arg146=
ENST00000703987.1:c.437G=	ENSP00000515604.1:p.Arg146=
ENST00000704649.1:c.437G=	ENSP00000515974.1:p.Arg146=
ENST00000704650.1:c.437G=	ENSP00000515975.1:p.Arg146=
ENST00000704651.1:c.437G=	ENSP00000515976.1:p.Arg146=
ENST00000324545.9:c.437G=	ENSP00000316357.6:p.Arg146=
ENST00000378308.7:c.437G= MANE Select	ENSP00000367558.2:p.Arg146=
ENST00000324545.8:c.437G=	ENSP00000316357.6:p.Arg146=
ENST00000378308.6:c.437G=	ENSP00000367558.2:p.Arg146=
NM_001039590.2:c.437G=	NP_001034679.2:p.Arg146=
NM_001039591.2:c.437G=	NP_001034680.2:p.Arg146=
XM_005272675.3:c.437G=	XP_005272732.1:p.Arg146=
XM_005272676.3:c.437G=	XP_005272733.1:p.Arg146=
XM_005272675.4:c.437G=	XP_005272732.1:p.Arg146=
XM_005272676.4:c.437G=	XP_005272733.1:p.Arg146=
NM_001039591.3:c.437G= MANE Select	NP_001034680.2:p.Arg146=
NM_001039590.3:c.437G=	NP_001034679.2:p.Arg146=