Canonical Allele Identifier: CA2425838800

Gene: USP9X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41230618C= , CM000685.2:g.41230618C=	GRCh38
NC_000023.10:g.41089871C= , CM000685.1:g.41089871C=	GRCh37
NC_000023.9:g.40974815C=	NCBI36
NG_012547.1:g.149984C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7542+22C=	ENSP00000515603.1:n.7542+22C=
ENST00000703987.1:c.7590+22C=	ENSP00000515604.1:n.7590+22C=
ENST00000704649.1:c.3685-1769C=	ENSP00000515974.1:n.3685-1769C=
ENST00000704650.1:c.7527+22C=	ENSP00000515975.1:n.7527+22C=
ENST00000704651.1:c.7374+22C=	ENSP00000515976.1:n.7374+22C=
ENST00000704652.1:c.6626+22C=
ENST00000704654.1:c.4406+22C=
ENST00000704655.1:c.3670+22C=	ENSP00000515980.1:n.3670+22C=
ENST00000704656.1:c.2978+22C=	ENSP00000515981.1:n.2978+22C=
ENST00000324545.9:c.7575+22C=	ENSP00000316357.6:n.7575+22C=
ENST00000378308.7:c.7527+22C= MANE Select	ENSP00000367558.2:n.7527+22C=
ENST00000324545.8:c.7575+22C=	ENSP00000316357.6:n.7575+22C=
ENST00000378308.6:c.7527+22C=	ENSP00000367558.2:n.7527+22C=
NM_001039590.2:c.7575+22C=	NP_001034679.2:n.7575+22C=
NM_001039591.2:c.7527+22C=	NP_001034680.2:n.7527+22C=
XM_005272675.3:c.7590+22C=	XP_005272732.1:n.7590+22C=
XM_005272676.3:c.7542+22C=	XP_005272733.1:n.7542+22C=
XM_005272675.4:c.7590+22C=	XP_005272732.1:n.7590+22C=
XM_005272676.4:c.7542+22C=	XP_005272733.1:n.7542+22C=
NM_001039591.3:c.7527+22C= MANE Select	NP_001034680.2:n.7527+22C=
NM_001039590.3:c.7575+22C=	NP_001034679.2:n.7575+22C=