Canonical Allele Identifier: CA2425838789

Gene: USP9X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41230591C= , CM000685.2:g.41230591C=	GRCh38
NC_000023.10:g.41089844C= , CM000685.1:g.41089844C=	GRCh37
NC_000023.9:g.40974788C=	NCBI36
NG_012547.1:g.149957C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7537C=	ENSP00000515603.1:p.Gln2513=
ENST00000703987.1:c.7585C=	ENSP00000515604.1:p.Gln2529=
ENST00000704649.1:c.3685-1796C=	ENSP00000515974.1:n.3685-1796C=
ENST00000704650.1:c.7522C=	ENSP00000515975.1:p.Gln2508=
ENST00000704651.1:c.7369C=	ENSP00000515976.1:p.Gln2457=
ENST00000704652.1:c.6621C=
ENST00000704654.1:c.4401C=
ENST00000704655.1:c.3665C=	ENSP00000515980.1:n.3665C=
ENST00000704656.1:c.2973C=	ENSP00000515981.1:n.2973C=
ENST00000324545.9:c.7570C=	ENSP00000316357.6:p.Gln2524=
ENST00000378308.7:c.7522C= MANE Select	ENSP00000367558.2:p.Gln2508=
ENST00000324545.8:c.7570C=	ENSP00000316357.6:p.Gln2524=
ENST00000378308.6:c.7522C=	ENSP00000367558.2:p.Gln2508=
NM_001039590.2:c.7570C=	NP_001034679.2:p.Gln2524=
NM_001039591.2:c.7522C=	NP_001034680.2:p.Gln2508=
XM_005272675.3:c.7585C=	XP_005272732.1:p.Gln2529=
XM_005272676.3:c.7537C=	XP_005272733.1:p.Gln2513=
XM_005272675.4:c.7585C=	XP_005272732.1:p.Gln2529=
XM_005272676.4:c.7537C=	XP_005272733.1:p.Gln2513=
NM_001039591.3:c.7522C= MANE Select	NP_001034680.2:p.Gln2508=
NM_001039590.3:c.7570C=	NP_001034679.2:p.Gln2524=