Canonical Allele Identifier: CA658684297

Gene: USP9X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41201212del , CM000685.2:g.41201212del	GRCh38
NC_000023.10:g.41060465del , CM000685.1:g.41060465del	GRCh37
NC_000023.9:g.40945409del	NCBI36
NG_012547.1:g.120578del

Transcript Alleles

HGVS	Amino-acid Change
NM_001039591.3:c.4756del MANE Select	NP_001034680.2:p.Ala1587ProfsTer9
ENST00000378308.7:c.4756del MANE Select	ENSP00000367558.2:p.Ala1587ProfsTer9
NM_001039590.2:c.4756del	NP_001034679.2:p.Ala1587ProfsTer9
NM_001039590.3:c.4756del	NP_001034679.2:p.Ala1587ProfsTer9
NM_001039591.2:c.4756del	NP_001034680.2:p.Ala1587ProfsTer9
ENST00000324545.8:c.4756del	ENSP00000316357.6:p.Ala1587ProfsTer9
ENST00000324545.9:c.4756del	ENSP00000316357.6:p.Ala1587ProfsTer9
ENST00000378308.6:c.4756del	ENSP00000367558.2:p.Ala1587ProfsTer9
ENST00000703986.1:c.4771del	ENSP00000515603.1:p.Ala1592ProfsTer9
ENST00000703987.1:c.4771del	ENSP00000515604.1:p.Ala1592ProfsTer9
ENST00000704649.1:c.3684+14570del	ENSP00000515974.1:n.3684+14570del
ENST00000704650.1:c.4756del	ENSP00000515975.1:p.Ala1587ProfsTer9
ENST00000704651.1:c.4603del	ENSP00000515976.1:p.Ala1536ProfsTer9
ENST00000704652.1:c.3855del
ENST00000704654.1:c.1710del
ENST00000704655.1:c.946del	ENSP00000515980.1:p.Ala317ProfsTer9
ENST00000704656.1:c.523del	ENSP00000515981.1:p.Ala176ProfsTer9
XM_005272675.3:c.4771del	XP_005272732.1:p.Ala1592ProfsTer9
XM_005272675.4:c.4771del	XP_005272732.1:p.Ala1592ProfsTer9
XM_005272676.3:c.4771del	XP_005272733.1:p.Ala1592ProfsTer9
XM_005272676.4:c.4771del	XP_005272733.1:p.Ala1592ProfsTer9