Canonical Allele Identifier: CA412754643

Gene: USP9X

Linked Data

• MyVariant Identifiers: chrX:g.41089816G>T (hg19) ; chrX:g.41230563G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41230563G>T , CM000685.2:g.41230563G>T	GRCh38
NC_000023.10:g.41089816G>T , CM000685.1:g.41089816G>T	GRCh37
NC_000023.9:g.40974760G>T	NCBI36
NG_012547.1:g.149929G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7509G>T	ENSP00000515603.1:p.Leu2503Phe
ENST00000703987.1:c.7557G>T	ENSP00000515604.1:p.Leu2519Phe
ENST00000704649.1:c.3685-1824G>T	ENSP00000515974.1:n.3685-1824G>T
ENST00000704650.1:c.7494G>T	ENSP00000515975.1:p.Leu2498Phe
ENST00000704651.1:c.7341G>T	ENSP00000515976.1:p.Leu2447Phe
ENST00000704652.1:c.6593G>T
ENST00000704654.1:c.4373G>T
ENST00000704655.1:c.3637G>T	ENSP00000515980.1:n.3637G>T
ENST00000704656.1:c.2945G>T	ENSP00000515981.1:n.2945G>T
ENST00000324545.9:c.7542G>T	ENSP00000316357.6:p.Leu2514Phe
ENST00000378308.7:c.7494G>T MANE Select	ENSP00000367558.2:p.Leu2498Phe
ENST00000324545.8:c.7542G>T	ENSP00000316357.6:p.Leu2514Phe
ENST00000378308.6:c.7494G>T	ENSP00000367558.2:p.Leu2498Phe
NM_001039590.2:c.7542G>T	NP_001034679.2:p.Leu2514Phe
NM_001039591.2:c.7494G>T	NP_001034680.2:p.Leu2498Phe
XM_005272675.3:c.7557G>T	XP_005272732.1:p.Leu2519Phe
XM_005272676.3:c.7509G>T	XP_005272733.1:p.Leu2503Phe
XM_005272675.4:c.7557G>T	XP_005272732.1:p.Leu2519Phe
XM_005272676.4:c.7509G>T	XP_005272733.1:p.Leu2503Phe
NM_001039591.3:c.7494G>T MANE Select	NP_001034680.2:p.Leu2498Phe
NM_001039590.3:c.7542G>T	NP_001034679.2:p.Leu2514Phe