Canonical Allele Identifier: CA516347752

Gene: USP9X

Linked Data

• MyVariant Identifiers: chrX:g.41088560A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41229307A>T , CM000685.2:g.41229307A>T	GRCh38
NC_000023.10:g.41088560A>T , CM000685.1:g.41088560A>T	GRCh37
NC_000023.9:g.40973504A>T	NCBI36
NG_012547.1:g.148673A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703986.1:c.7131A>T	ENSP00000515603.1:p.Thr2377=
ENST00000703987.1:c.7131A>T	ENSP00000515604.1:p.Thr2377=
ENST00000704649.1:c.3685-3080A>T	ENSP00000515974.1:n.3685-3080A>T
ENST00000704650.1:c.7116A>T	ENSP00000515975.1:p.Thr2372=
ENST00000704651.1:c.6963A>T	ENSP00000515976.1:p.Thr2321=
ENST00000704652.1:c.6215A>T
ENST00000704654.1:c.3995A>T
ENST00000704655.1:c.3259A>T	ENSP00000515980.1:n.3259A>T
ENST00000704656.1:c.2567A>T	ENSP00000515981.1:n.2567A>T
ENST00000324545.9:c.7116A>T	ENSP00000316357.6:p.Thr2372=
ENST00000378308.7:c.7116A>T MANE Select	ENSP00000367558.2:p.Thr2372=
ENST00000324545.8:c.7116A>T	ENSP00000316357.6:p.Thr2372=
ENST00000378308.6:c.7116A>T	ENSP00000367558.2:p.Thr2372=
ENST00000485180.1:n.325A>T
NM_001039590.2:c.7116A>T	NP_001034679.2:p.Thr2372=
NM_001039591.2:c.7116A>T	NP_001034680.2:p.Thr2372=
XM_005272675.3:c.7131A>T	XP_005272732.1:p.Thr2377=
XM_005272676.3:c.7131A>T	XP_005272733.1:p.Thr2377=
XM_005272675.4:c.7131A>T	XP_005272732.1:p.Thr2377=
XM_005272676.4:c.7131A>T	XP_005272733.1:p.Thr2377=
NM_001039591.3:c.7116A>T MANE Select	NP_001034680.2:p.Thr2372=
NM_001039590.3:c.7116A>T	NP_001034679.2:p.Thr2372=