Canonical Allele Identifier: CA875373629

Gene: USP9X

Linked Data

• dbSNP Id: rs1264331735
• gnomAD v4: X-41230479-A-G
• MyVariant Identifiers: chrX:g.41089732A>G (hg19) ; chrX:g.41230479A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41230479A>G , CM000685.2:g.41230479A>G	GRCh38
NC_000023.10:g.41089732A>G , CM000685.1:g.41089732A>G	GRCh37
NC_000023.9:g.40974676A>G	NCBI36
NG_012547.1:g.149845A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7447-22A>G	ENSP00000515603.1:n.7447-22A>G
ENST00000703987.1:c.7495-22A>G	ENSP00000515604.1:n.7495-22A>G
ENST00000704649.1:c.3685-1908A>G	ENSP00000515974.1:n.3685-1908A>G
ENST00000704650.1:c.7432-22A>G	ENSP00000515975.1:n.7432-22A>G
ENST00000704651.1:c.7279-22A>G	ENSP00000515976.1:n.7279-22A>G
ENST00000704652.1:c.6531-22A>G
ENST00000704654.1:c.4311-22A>G
ENST00000704655.1:c.3575-22A>G	ENSP00000515980.1:n.3575-22A>G
ENST00000704656.1:c.2883-22A>G	ENSP00000515981.1:n.2883-22A>G
ENST00000324545.9:c.7480-22A>G	ENSP00000316357.6:n.7480-22A>G
ENST00000378308.7:c.7432-22A>G MANE Select	ENSP00000367558.2:n.7432-22A>G
ENST00000324545.8:c.7480-22A>G	ENSP00000316357.6:n.7480-22A>G
ENST00000378308.6:c.7432-22A>G	ENSP00000367558.2:n.7432-22A>G
NM_001039590.2:c.7480-22A>G	NP_001034679.2:n.7480-22A>G
NM_001039591.2:c.7432-22A>G	NP_001034680.2:n.7432-22A>G
XM_005272675.3:c.7495-22A>G	XP_005272732.1:n.7495-22A>G
XM_005272676.3:c.7447-22A>G	XP_005272733.1:n.7447-22A>G
XM_005272675.4:c.7495-22A>G	XP_005272732.1:n.7495-22A>G
XM_005272676.4:c.7447-22A>G	XP_005272733.1:n.7447-22A>G
NM_001039591.3:c.7432-22A>G MANE Select	NP_001034680.2:n.7432-22A>G
NM_001039590.3:c.7480-22A>G	NP_001034679.2:n.7480-22A>G