Canonical Allele Identifier: CA10389184

Gene: USP9X

Linked Data

• dbSNP Id: rs773038017
• ExAC: X:41088497 C / G
• gnomAD v2: X-41088497-C-G
• gnomAD v3: X-41229244-C-G
• gnomAD v4: X-41229244-C-G
• MyVariant Identifiers: chrX:g.41088497C>G (hg19) ; chrX:g.41229244C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41229244C>G , CM000685.2:g.41229244C>G	GRCh38
NC_000023.10:g.41088497C>G , CM000685.1:g.41088497C>G	GRCh37
NC_000023.9:g.40973441C>G	NCBI36
NG_012547.1:g.148610C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7077-9C>G	ENSP00000515603.1:n.7077-9C>G
ENST00000703987.1:c.7077-9C>G	ENSP00000515604.1:n.7077-9C>G
ENST00000704649.1:c.3685-3143C>G	ENSP00000515974.1:n.3685-3143C>G
ENST00000704650.1:c.7062-9C>G	ENSP00000515975.1:n.7062-9C>G
ENST00000704651.1:c.6909-9C>G	ENSP00000515976.1:n.6909-9C>G
ENST00000704652.1:c.6161-9C>G
ENST00000704654.1:c.3941-9C>G
ENST00000704655.1:c.3205-9C>G	ENSP00000515980.1:n.3205-9C>G
ENST00000704656.1:c.2513-9C>G	ENSP00000515981.1:n.2513-9C>G
ENST00000324545.9:c.7062-9C>G	ENSP00000316357.6:n.7062-9C>G
ENST00000378308.7:c.7062-9C>G MANE Select	ENSP00000367558.2:n.7062-9C>G
ENST00000324545.8:c.7062-9C>G	ENSP00000316357.6:n.7062-9C>G
ENST00000378308.6:c.7062-9C>G	ENSP00000367558.2:n.7062-9C>G
ENST00000485180.1:n.262C>G
NM_001039590.2:c.7062-9C>G	NP_001034679.2:n.7062-9C>G
NM_001039591.2:c.7062-9C>G	NP_001034680.2:n.7062-9C>G
XM_005272675.3:c.7077-9C>G	XP_005272732.1:n.7077-9C>G
XM_005272676.3:c.7077-9C>G	XP_005272733.1:n.7077-9C>G
XM_005272675.4:c.7077-9C>G	XP_005272732.1:n.7077-9C>G
XM_005272676.4:c.7077-9C>G	XP_005272733.1:n.7077-9C>G
NM_001039591.3:c.7062-9C>G MANE Select	NP_001034680.2:n.7062-9C>G
NM_001039590.3:c.7062-9C>G	NP_001034679.2:n.7062-9C>G