Canonical Allele Identifier: CA16621373

Gene: USP9X

Linked Data

• ClinVar Variation Id: 422179
• ClinVar RCV Id: RCV000482190
• dbSNP Id: rs1064795608
• MyVariant Identifiers: chrX:g.41002685T>C (hg19) ; chrX:g.41143432T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41143432T>C , CM000685.2:g.41143432T>C	GRCh38
NC_000023.10:g.41002685T>C , CM000685.1:g.41002685T>C	GRCh37
NC_000023.9:g.40887629T>C	NCBI36
NG_012547.1:g.62798T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703986.1:c.1303T>C	ENSP00000515603.1:p.Trp435Arg
ENST00000703987.1:c.1303T>C	ENSP00000515604.1:p.Trp435Arg
ENST00000704649.1:c.1303T>C	ENSP00000515974.1:p.Trp435Arg
ENST00000704650.1:c.1303T>C	ENSP00000515975.1:p.Trp435Arg
ENST00000704651.1:c.1162-1090T>C	ENSP00000515976.1:n.1162-1090T>C
ENST00000704652.1:c.533T>C
ENST00000324545.9:c.1303T>C	ENSP00000316357.6:p.Trp435Arg
ENST00000378308.7:c.1303T>C MANE Select	ENSP00000367558.2:p.Trp435Arg
ENST00000324545.8:c.1303T>C	ENSP00000316357.6:p.Trp435Arg
ENST00000378308.6:c.1303T>C	ENSP00000367558.2:p.Trp435Arg
NM_001039590.2:c.1303T>C	NP_001034679.2:p.Trp435Arg
NM_001039591.2:c.1303T>C	NP_001034680.2:p.Trp435Arg
XM_005272675.3:c.1303T>C	XP_005272732.1:p.Trp435Arg
XM_005272676.3:c.1303T>C	XP_005272733.1:p.Trp435Arg
XM_005272675.4:c.1303T>C	XP_005272732.1:p.Trp435Arg
XM_005272676.4:c.1303T>C	XP_005272733.1:p.Trp435Arg
NM_001039591.3:c.1303T>C MANE Select	NP_001034680.2:p.Trp435Arg
NM_001039590.3:c.1303T>C	NP_001034679.2:p.Trp435Arg