Canonical Allele Identifier: CA2580100867

Gene: USP9X

Linked Data

• ClinVar Variation Id: 1703492
• ClinVar RCV Id: RCV002280069

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41229379dup , CM000685.2:g.41229379dup	GRCh38
NC_000023.10:g.41088632dup , CM000685.1:g.41088632dup	GRCh37
NC_000023.9:g.40973576dup	NCBI36
NG_012547.1:g.148745dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7203dup	ENSP00000515603.1:p.Asn2402Ter
ENST00000703987.1:c.7203dup	ENSP00000515604.1:p.Asn2402Ter
ENST00000704649.1:c.3685-3008dup	ENSP00000515974.1:n.3685-3008dup
ENST00000704650.1:c.7188dup	ENSP00000515975.1:p.Asn2397Ter
ENST00000704651.1:c.7035dup	ENSP00000515976.1:p.Asn2346Ter
ENST00000704652.1:c.6287dup
ENST00000704654.1:c.4067dup
ENST00000704655.1:c.3331dup	ENSP00000515980.1:n.3331dup
ENST00000704656.1:c.2639dup	ENSP00000515981.1:n.2639dup
ENST00000324545.9:c.7188dup	ENSP00000316357.6:p.Asn2397Ter
ENST00000378308.7:c.7188dup MANE Select	ENSP00000367558.2:p.Asn2397Ter
ENST00000324545.8:c.7188dup	ENSP00000316357.6:p.Asn2397Ter
ENST00000378308.6:c.7188dup	ENSP00000367558.2:p.Asn2397Ter
ENST00000485180.1:n.397dup
NM_001039590.2:c.7188dup	NP_001034679.2:p.Asn2397Ter
NM_001039591.2:c.7188dup	NP_001034680.2:p.Asn2397Ter
XM_005272675.3:c.7203dup	XP_005272732.1:p.Asn2402Ter
XM_005272676.3:c.7203dup	XP_005272733.1:p.Asn2402Ter
XM_005272675.4:c.7203dup	XP_005272732.1:p.Asn2402Ter
XM_005272676.4:c.7203dup	XP_005272733.1:p.Asn2402Ter
NM_001039591.3:c.7188dup MANE Select	NP_001034680.2:p.Asn2397Ter
NM_001039590.3:c.7188dup	NP_001034679.2:p.Asn2397Ter