Canonical Allele Identifier: CA2425806578

Gene: USP9X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41136792C= , CM000685.2:g.41136792C=	GRCh38
NC_000023.10:g.40996045C= , CM000685.1:g.40996045C=	GRCh37
NC_000023.9:g.40880989C=	NCBI36
NG_012547.1:g.56158C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000703986.1:c.436-12C=	ENSP00000515603.1:n.436-12C=
ENST00000703987.1:c.436-12C=	ENSP00000515604.1:n.436-12C=
ENST00000704649.1:c.436-12C=	ENSP00000515974.1:n.436-12C=
ENST00000704650.1:c.436-12C=	ENSP00000515975.1:n.436-12C=
ENST00000704651.1:c.436-12C=	ENSP00000515976.1:n.436-12C=
ENST00000324545.9:c.436-12C=	ENSP00000316357.6:n.436-12C=
ENST00000378308.7:c.436-12C= MANE Select	ENSP00000367558.2:n.436-12C=
ENST00000324545.8:c.436-12C=	ENSP00000316357.6:n.436-12C=
ENST00000378308.6:c.436-12C=	ENSP00000367558.2:n.436-12C=
NM_001039590.2:c.436-12C=	NP_001034679.2:n.436-12C=
NM_001039591.2:c.436-12C=	NP_001034680.2:n.436-12C=
XM_005272675.3:c.436-12C=	XP_005272732.1:n.436-12C=
XM_005272676.3:c.436-12C=	XP_005272733.1:n.436-12C=
XM_005272675.4:c.436-12C=	XP_005272732.1:n.436-12C=
XM_005272676.4:c.436-12C=	XP_005272733.1:n.436-12C=
NM_001039591.3:c.436-12C= MANE Select	NP_001034680.2:n.436-12C=
NM_001039590.3:c.436-12C=	NP_001034679.2:n.436-12C=