Canonical Allele Identifier: CA2425833529

Gene: USP9X

Linked Data

• dbSNP Id: rs1783377757

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41214501A>C , CM000685.2:g.41214501A>C	GRCh38
NC_000023.10:g.41073754A>C , CM000685.1:g.41073754A>C	GRCh37
NC_000023.9:g.40958698A>C	NCBI36
NG_012547.1:g.133867A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000703986.1:c.5205-67A>C	ENSP00000515603.1:n.5205-67A>C
ENST00000703987.1:c.5205-67A>C	ENSP00000515604.1:n.5205-67A>C
ENST00000704649.1:c.3685-17886A>C	ENSP00000515974.1:n.3685-17886A>C
ENST00000704650.1:c.5190-67A>C	ENSP00000515975.1:n.5190-67A>C
ENST00000704651.1:c.5037-67A>C	ENSP00000515976.1:n.5037-67A>C
ENST00000704652.1:c.4289-67A>C
ENST00000704654.1:c.2144-67A>C
ENST00000704655.1:c.1333-67A>C	ENSP00000515980.1:n.1333-67A>C
ENST00000704656.1:c.783-1398A>C	ENSP00000515981.1:n.783-1398A>C
ENST00000324545.9:c.5190-67A>C	ENSP00000316357.6:n.5190-67A>C
ENST00000378308.7:c.5190-67A>C MANE Select	ENSP00000367558.2:n.5190-67A>C
ENST00000324545.8:c.5190-67A>C	ENSP00000316357.6:n.5190-67A>C
ENST00000378308.6:c.5190-67A>C	ENSP00000367558.2:n.5190-67A>C
NM_001039590.2:c.5190-67A>C	NP_001034679.2:n.5190-67A>C
NM_001039591.2:c.5190-67A>C	NP_001034680.2:n.5190-67A>C
XM_005272675.3:c.5205-67A>C	XP_005272732.1:n.5205-67A>C
XM_005272676.3:c.5205-67A>C	XP_005272733.1:n.5205-67A>C
XM_005272675.4:c.5205-67A>C	XP_005272732.1:n.5205-67A>C
XM_005272676.4:c.5205-67A>C	XP_005272733.1:n.5205-67A>C
NM_001039591.3:c.5190-67A>C MANE Select	NP_001034680.2:n.5190-67A>C
NM_001039590.3:c.5190-67A>C	NP_001034679.2:n.5190-67A>C