Canonical Allele Identifier: CA412752206

Gene: USP9X

Linked Data

• gnomAD v4: X-41229348-A-G
• MyVariant Identifiers: chrX:g.41088601A>G (hg19) ; chrX:g.41229348A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41229348A>G , CM000685.2:g.41229348A>G	GRCh38
NC_000023.10:g.41088601A>G , CM000685.1:g.41088601A>G	GRCh37
NC_000023.9:g.40973545A>G	NCBI36
NG_012547.1:g.148714A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.7172A>G	ENSP00000515603.1:p.Gln2391Arg
ENST00000703987.1:c.7172A>G	ENSP00000515604.1:p.Gln2391Arg
ENST00000704649.1:c.3685-3039A>G	ENSP00000515974.1:n.3685-3039A>G
ENST00000704650.1:c.7157A>G	ENSP00000515975.1:p.Gln2386Arg
ENST00000704651.1:c.7004A>G	ENSP00000515976.1:p.Gln2335Arg
ENST00000704652.1:c.6256A>G
ENST00000704654.1:c.4036A>G
ENST00000704655.1:c.3300A>G	ENSP00000515980.1:n.3300A>G
ENST00000704656.1:c.2608A>G	ENSP00000515981.1:n.2608A>G
ENST00000324545.9:c.7157A>G	ENSP00000316357.6:p.Gln2386Arg
ENST00000378308.7:c.7157A>G MANE Select	ENSP00000367558.2:p.Gln2386Arg
ENST00000324545.8:c.7157A>G	ENSP00000316357.6:p.Gln2386Arg
ENST00000378308.6:c.7157A>G	ENSP00000367558.2:p.Gln2386Arg
ENST00000485180.1:n.366A>G
NM_001039590.2:c.7157A>G	NP_001034679.2:p.Gln2386Arg
NM_001039591.2:c.7157A>G	NP_001034680.2:p.Gln2386Arg
XM_005272675.3:c.7172A>G	XP_005272732.1:p.Gln2391Arg
XM_005272676.3:c.7172A>G	XP_005272733.1:p.Gln2391Arg
XM_005272675.4:c.7172A>G	XP_005272732.1:p.Gln2391Arg
XM_005272676.4:c.7172A>G	XP_005272733.1:p.Gln2391Arg
NM_001039591.3:c.7157A>G MANE Select	NP_001034680.2:p.Gln2386Arg
NM_001039590.3:c.7157A>G	NP_001034679.2:p.Gln2386Arg