Canonical Allele Identifier: CA412787530

Gene: USP9X

Linked Data

• MyVariant Identifiers: chrX:g.41073855G>T (hg19) ; chrX:g.41214602G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41214602G>T , CM000685.2:g.41214602G>T	GRCh38
NC_000023.10:g.41073855G>T , CM000685.1:g.41073855G>T	GRCh37
NC_000023.9:g.40958799G>T	NCBI36
NG_012547.1:g.133968G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703986.1:c.5239G>T	ENSP00000515603.1:p.Val1747Leu
ENST00000703987.1:c.5239G>T	ENSP00000515604.1:p.Val1747Leu
ENST00000704649.1:c.3685-17785G>T	ENSP00000515974.1:n.3685-17785G>T
ENST00000704650.1:c.5224G>T	ENSP00000515975.1:p.Val1742Leu
ENST00000704651.1:c.5071G>T	ENSP00000515976.1:p.Val1691Leu
ENST00000704652.1:c.4323G>T
ENST00000704654.1:c.2178G>T
ENST00000704655.1:c.1367G>T	ENSP00000515980.1:n.1367G>T
ENST00000704656.1:c.783-1297G>T	ENSP00000515981.1:n.783-1297G>T
ENST00000324545.9:c.5224G>T	ENSP00000316357.6:p.Val1742Leu
ENST00000378308.7:c.5224G>T MANE Select	ENSP00000367558.2:p.Val1742Leu
ENST00000324545.8:c.5224G>T	ENSP00000316357.6:p.Val1742Leu
ENST00000378308.6:c.5224G>T	ENSP00000367558.2:p.Val1742Leu
NM_001039590.2:c.5224G>T	NP_001034679.2:p.Val1742Leu
NM_001039591.2:c.5224G>T	NP_001034680.2:p.Val1742Leu
XM_005272675.3:c.5239G>T	XP_005272732.1:p.Val1747Leu
XM_005272676.3:c.5239G>T	XP_005272733.1:p.Val1747Leu
XM_005272675.4:c.5239G>T	XP_005272732.1:p.Val1747Leu
XM_005272676.4:c.5239G>T	XP_005272733.1:p.Val1747Leu
NM_001039591.3:c.5224G>T MANE Select	NP_001034680.2:p.Val1742Leu
NM_001039590.3:c.5224G>T	NP_001034679.2:p.Val1742Leu