Canonical Allele Identifier: CA412799943

Gene: USP9X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41218472C>A , CM000685.2:g.41218472C>A	GRCh38
NC_000023.10:g.41077725C>A , CM000685.1:g.41077725C>A	GRCh37
NC_000023.9:g.40962669C>A	NCBI36
NG_012547.1:g.137838C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001039591.3:c.6310C>A MANE Select	NP_001034680.2:p.Leu2104Ile
ENST00000378308.7:c.6310C>A MANE Select	ENSP00000367558.2:p.Leu2104Ile
NM_001039590.2:c.6310C>A	NP_001034679.2:p.Leu2104Ile
NM_001039590.3:c.6310C>A	NP_001034679.2:p.Leu2104Ile
NM_001039591.2:c.6310C>A	NP_001034680.2:p.Leu2104Ile
ENST00000324545.8:c.6310C>A	ENSP00000316357.6:p.Leu2104Ile
ENST00000324545.9:c.6310C>A	ENSP00000316357.6:p.Leu2104Ile
ENST00000378308.6:c.6310C>A	ENSP00000367558.2:p.Leu2104Ile
ENST00000703986.1:c.6325C>A	ENSP00000515603.1:p.Leu2109Ile
ENST00000703987.1:c.6325C>A	ENSP00000515604.1:p.Leu2109Ile
ENST00000704649.1:c.3685-13915C>A	ENSP00000515974.1:n.3685-13915C>A
ENST00000704650.1:c.6310C>A	ENSP00000515975.1:p.Leu2104Ile
ENST00000704651.1:c.6157C>A	ENSP00000515976.1:p.Leu2053Ile
ENST00000704652.1:c.5409C>A
ENST00000704654.1:c.3264C>A
ENST00000704655.1:c.2453C>A	ENSP00000515980.1:n.2453C>A
ENST00000704656.1:c.1761C>A	ENSP00000515981.1:n.1761C>A
XM_005272675.3:c.6325C>A	XP_005272732.1:p.Leu2109Ile
XM_005272675.4:c.6325C>A	XP_005272732.1:p.Leu2109Ile
XM_005272676.3:c.6325C>A	XP_005272733.1:p.Leu2109Ile
XM_005272676.4:c.6325C>A	XP_005272733.1:p.Leu2109Ile