Canonical Allele Identifier: CA412768968

Gene: USP9X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41189393A>C , CM000685.2:g.41189393A>C	GRCh38
NC_000023.10:g.41048646A>C , CM000685.1:g.41048646A>C	GRCh37
NC_000023.9:g.40933590A>C	NCBI36
NG_012547.1:g.108759A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001039591.3:c.3895A>C MANE Select	NP_001034680.2:p.Ile1299Leu
ENST00000378308.7:c.3895A>C MANE Select	ENSP00000367558.2:p.Ile1299Leu
NM_001039590.2:c.3895A>C	NP_001034679.2:p.Ile1299Leu
NM_001039590.3:c.3895A>C	NP_001034679.2:p.Ile1299Leu
NM_001039591.2:c.3895A>C	NP_001034680.2:p.Ile1299Leu
ENST00000324545.8:c.3895A>C	ENSP00000316357.6:p.Ile1299Leu
ENST00000324545.9:c.3895A>C	ENSP00000316357.6:p.Ile1299Leu
ENST00000378308.6:c.3895A>C	ENSP00000367558.2:p.Ile1299Leu
ENST00000463829.1:n.137A>C
ENST00000703986.1:c.3910A>C	ENSP00000515603.1:p.Ile1304Leu
ENST00000703987.1:c.3910A>C	ENSP00000515604.1:p.Ile1304Leu
ENST00000704649.1:c.3684+2751A>C	ENSP00000515974.1:n.3684+2751A>C
ENST00000704650.1:c.3895A>C	ENSP00000515975.1:p.Ile1299Leu
ENST00000704651.1:c.3742A>C	ENSP00000515976.1:p.Ile1248Leu
ENST00000704652.1:c.2994A>C
ENST00000704654.1:c.849A>C
ENST00000704655.1:c.85A>C	ENSP00000515980.1:p.Ile29Leu
XM_005272675.3:c.3910A>C	XP_005272732.1:p.Ile1304Leu
XM_005272675.4:c.3910A>C	XP_005272732.1:p.Ile1304Leu
XM_005272676.3:c.3910A>C	XP_005272733.1:p.Ile1304Leu
XM_005272676.4:c.3910A>C	XP_005272733.1:p.Ile1304Leu