Canonical Allele Identifier: CA412761954
Gene: USP9X HGNC NCBI

Linked Data

ClinVar Variation Id: 427036
ClinVar RCV Id: RCV000489858
dbSNP Id: rs1085307914
MyVariant Identifiers: chrX:g.40994047T>A (hg19) chrX:g.41134794T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41134794T>A , CM000685.2:g.41134794T>A GRCh38
NC_000023.10:g.40994047T>A , CM000685.1:g.40994047T>A GRCh37
NC_000023.9:g.40878991T>A NCBI36
NG_012547.1:g.54160T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703986.1:c.392T>A ENSP00000515603.1:p.Ile131Asn
ENST00000703987.1:c.392T>A ENSP00000515604.1:p.Ile131Asn
ENST00000704649.1:c.392T>A ENSP00000515974.1:p.Ile131Asn
ENST00000704650.1:c.392T>A ENSP00000515975.1:p.Ile131Asn
ENST00000704651.1:c.392T>A ENSP00000515976.1:p.Ile131Asn
ENST00000324545.9:c.392T>A ENSP00000316357.6:p.Ile131Asn
ENST00000378308.7:c.392T>A MANE Select ENSP00000367558.2:p.Ile131Asn
ENST00000324545.8:c.392T>A ENSP00000316357.6:p.Ile131Asn
ENST00000378308.6:c.392T>A ENSP00000367558.2:p.Ile131Asn
NM_001039590.2:c.392T>A NP_001034679.2:p.Ile131Asn
NM_001039591.2:c.392T>A NP_001034680.2:p.Ile131Asn
XM_005272675.3:c.392T>A XP_005272732.1:p.Ile131Asn
XM_005272676.3:c.392T>A XP_005272733.1:p.Ile131Asn
XM_005272675.4:c.392T>A XP_005272732.1:p.Ile131Asn
XM_005272676.4:c.392T>A XP_005272733.1:p.Ile131Asn
NM_001039591.3:c.392T>A MANE Select NP_001034680.2:p.Ile131Asn
NM_001039590.3:c.392T>A NP_001034679.2:p.Ile131Asn
Search 100 bp 5'
Search 100 bp 3'