Canonical Allele Identifier: CA412764420

Gene: USP9X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41184421G>A , CM000685.2:g.41184421G>A	GRCh38
NC_000023.10:g.41043674G>A , CM000685.1:g.41043674G>A	GRCh37
NC_000023.9:g.40928618G>A	NCBI36
NG_012547.1:g.103787G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001039591.3:c.3304G>A MANE Select	NP_001034680.2:p.Ala1102Thr
ENST00000378308.7:c.3304G>A MANE Select	ENSP00000367558.2:p.Ala1102Thr
NM_001039590.2:c.3304G>A	NP_001034679.2:p.Ala1102Thr
NM_001039590.3:c.3304G>A	NP_001034679.2:p.Ala1102Thr
NM_001039591.2:c.3304G>A	NP_001034680.2:p.Ala1102Thr
ENST00000324545.8:c.3304G>A	ENSP00000316357.6:p.Ala1102Thr
ENST00000324545.9:c.3304G>A	ENSP00000316357.6:p.Ala1102Thr
ENST00000378308.6:c.3304G>A	ENSP00000367558.2:p.Ala1102Thr
ENST00000465386.1:n.160G>A
ENST00000703986.1:c.3319G>A	ENSP00000515603.1:p.Ala1107Thr
ENST00000703987.1:c.3319G>A	ENSP00000515604.1:p.Ala1107Thr
ENST00000704649.1:c.3304G>A	ENSP00000515974.1:p.Ala1102Thr
ENST00000704650.1:c.3304G>A	ENSP00000515975.1:p.Ala1102Thr
ENST00000704651.1:c.3151G>A	ENSP00000515976.1:p.Ala1051Thr
ENST00000704652.1:c.2403G>A
ENST00000704654.1:c.258G>A
XM_005272675.3:c.3319G>A	XP_005272732.1:p.Ala1107Thr
XM_005272675.4:c.3319G>A	XP_005272732.1:p.Ala1107Thr
XM_005272676.3:c.3319G>A	XP_005272733.1:p.Ala1107Thr
XM_005272676.4:c.3319G>A	XP_005272733.1:p.Ala1107Thr