Canonical Allele Identifier: CA2425838724

Gene: USP9X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41230361C= , CM000685.2:g.41230361C=	GRCh38
NC_000023.10:g.41089614C= , CM000685.1:g.41089614C=	GRCh37
NC_000023.9:g.40974558C=	NCBI36
NG_012547.1:g.149727C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7447-140C=	ENSP00000515603.1:n.7447-140C=
ENST00000703987.1:c.7495-140C=	ENSP00000515604.1:n.7495-140C=
ENST00000704649.1:c.3685-2026C=	ENSP00000515974.1:n.3685-2026C=
ENST00000704650.1:c.7432-140C=	ENSP00000515975.1:n.7432-140C=
ENST00000704651.1:c.7279-140C=	ENSP00000515976.1:n.7279-140C=
ENST00000704652.1:c.6531-140C=
ENST00000704654.1:c.4311-140C=
ENST00000704655.1:c.3575-140C=	ENSP00000515980.1:n.3575-140C=
ENST00000704656.1:c.2883-140C=	ENSP00000515981.1:n.2883-140C=
ENST00000324545.9:c.7480-140C=	ENSP00000316357.6:n.7480-140C=
ENST00000378308.7:c.7432-140C= MANE Select	ENSP00000367558.2:n.7432-140C=
ENST00000324545.8:c.7480-140C=	ENSP00000316357.6:n.7480-140C=
ENST00000378308.6:c.7432-140C=	ENSP00000367558.2:n.7432-140C=
NM_001039590.2:c.7480-140C=	NP_001034679.2:n.7480-140C=
NM_001039591.2:c.7432-140C=	NP_001034680.2:n.7432-140C=
XM_005272675.3:c.7495-140C=	XP_005272732.1:n.7495-140C=
XM_005272676.3:c.7447-140C=	XP_005272733.1:n.7447-140C=
XM_005272675.4:c.7495-140C=	XP_005272732.1:n.7495-140C=
XM_005272676.4:c.7447-140C=	XP_005272733.1:n.7447-140C=
NM_001039591.3:c.7432-140C= MANE Select	NP_001034680.2:n.7432-140C=
NM_001039590.3:c.7480-140C=	NP_001034679.2:n.7480-140C=