Canonical Allele Identifier: CA516347743

Gene: USP9X

Linked Data

• MyVariant Identifiers: chrX:g.41088554T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41229301T>C , CM000685.2:g.41229301T>C	GRCh38
NC_000023.10:g.41088554T>C , CM000685.1:g.41088554T>C	GRCh37
NC_000023.9:g.40973498T>C	NCBI36
NG_012547.1:g.148667T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000703986.1:c.7125T>C	ENSP00000515603.1:p.Phe2375=
ENST00000703987.1:c.7125T>C	ENSP00000515604.1:p.Phe2375=
ENST00000704649.1:c.3685-3086T>C	ENSP00000515974.1:n.3685-3086T>C
ENST00000704650.1:c.7110T>C	ENSP00000515975.1:p.Phe2370=
ENST00000704651.1:c.6957T>C	ENSP00000515976.1:p.Phe2319=
ENST00000704652.1:c.6209T>C
ENST00000704654.1:c.3989T>C
ENST00000704655.1:c.3253T>C	ENSP00000515980.1:n.3253T>C
ENST00000704656.1:c.2561T>C	ENSP00000515981.1:n.2561T>C
ENST00000324545.9:c.7110T>C	ENSP00000316357.6:p.Phe2370=
ENST00000378308.7:c.7110T>C MANE Select	ENSP00000367558.2:p.Phe2370=
ENST00000324545.8:c.7110T>C	ENSP00000316357.6:p.Phe2370=
ENST00000378308.6:c.7110T>C	ENSP00000367558.2:p.Phe2370=
ENST00000485180.1:n.319T>C
NM_001039590.2:c.7110T>C	NP_001034679.2:p.Phe2370=
NM_001039591.2:c.7110T>C	NP_001034680.2:p.Phe2370=
XM_005272675.3:c.7125T>C	XP_005272732.1:p.Phe2375=
XM_005272676.3:c.7125T>C	XP_005272733.1:p.Phe2375=
XM_005272675.4:c.7125T>C	XP_005272732.1:p.Phe2375=
XM_005272676.4:c.7125T>C	XP_005272733.1:p.Phe2375=
NM_001039591.3:c.7110T>C MANE Select	NP_001034680.2:p.Phe2370=
NM_001039590.3:c.7110T>C	NP_001034679.2:p.Phe2370=