Canonical Allele Identifier: CA10389240

Gene: USP9X

Linked Data

• dbSNP Id: rs772686164
• ExAC: X:41089877 T / TC
• gnomAD v2: X-41089877-T-TC
• MyVariant Identifiers: chrX:g.41089877_41089878insC (hg19) ; chrX:g.41230624_41230625insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41230628dup , CM000685.2:g.41230628dup	GRCh38
NC_000023.10:g.41089881dup , CM000685.1:g.41089881dup	GRCh37
NC_000023.9:g.40974825dup	NCBI36
NG_012547.1:g.149994dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7542+32dup	ENSP00000515603.1:n.7542+32dup
ENST00000703987.1:c.7590+32dup	ENSP00000515604.1:n.7590+32dup
ENST00000704649.1:c.3685-1759dup	ENSP00000515974.1:n.3685-1759dup
ENST00000704650.1:c.7527+32dup	ENSP00000515975.1:n.7527+32dup
ENST00000704651.1:c.7374+32dup	ENSP00000515976.1:n.7374+32dup
ENST00000704652.1:c.6626+32dup
ENST00000704654.1:c.4406+32dup
ENST00000704655.1:c.3670+32dup	ENSP00000515980.1:n.3670+32dup
ENST00000704656.1:c.2978+32dup	ENSP00000515981.1:n.2978+32dup
ENST00000324545.9:c.7575+32dup	ENSP00000316357.6:n.7575+32dup
ENST00000378308.7:c.7527+32dup MANE Select	ENSP00000367558.2:n.7527+32dup
ENST00000324545.8:c.7575+32dup	ENSP00000316357.6:n.7575+32dup
ENST00000378308.6:c.7527+32dup	ENSP00000367558.2:n.7527+32dup
NM_001039590.2:c.7575+32dup	NP_001034679.2:n.7575+32dup
NM_001039591.2:c.7527+32dup	NP_001034680.2:n.7527+32dup
XM_005272675.3:c.7590+32dup	XP_005272732.1:n.7590+32dup
XM_005272676.3:c.7542+32dup	XP_005272733.1:n.7542+32dup
XM_005272675.4:c.7590+32dup	XP_005272732.1:n.7590+32dup
XM_005272676.4:c.7542+32dup	XP_005272733.1:n.7542+32dup
NM_001039591.3:c.7527+32dup MANE Select	NP_001034680.2:n.7527+32dup
NM_001039590.3:c.7575+32dup	NP_001034679.2:n.7575+32dup