Canonical Allele Identifier: CA16621375
Gene: USP9X HGNC NCBI

Linked Data

ClinVar Variation Id: 419674
ClinVar RCV Id: RCV000487109
dbSNP Id: rs1064794035
MyVariant Identifiers: chrX:g.41077780_41077781del (hg19) chrX:g.41218527_41218528del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41218527_41218528del , CM000685.2:g.41218527_41218528del GRCh38
NC_000023.10:g.41077780_41077781del , CM000685.1:g.41077780_41077781del GRCh37
NC_000023.9:g.40962724_40962725del NCBI36
NG_012547.1:g.137893_137894del

Transcript Alleles

HGVS Amino-acid change
ENST00000703986.1:c.6380_6381del ENSP00000515603.1:p.Phe2127TyrfsTer22
ENST00000703987.1:c.6380_6381del ENSP00000515604.1:p.Phe2127TyrfsTer22
ENST00000704649.1:c.3685-13860_3685-13859del ENSP00000515974.1:n.3685-13860_3685-13859...
ENST00000704650.1:c.6365_6366del ENSP00000515975.1:p.Phe2122TyrfsTer22
ENST00000704651.1:c.6212_6213del ENSP00000515976.1:p.Phe2071TyrfsTer22
ENST00000704652.1:c.5464_5465del
ENST00000704654.1:c.3319_3320del
ENST00000704655.1:c.2508_2509del ENSP00000515980.1:n.2508_2509del
ENST00000704656.1:c.1816_1817del ENSP00000515981.1:n.1816_1817del
ENST00000324545.9:c.6365_6366del ENSP00000316357.6:p.Phe2122TyrfsTer22
ENST00000378308.7:c.6365_6366del MANE Select ENSP00000367558.2:p.Phe2122TyrfsTer22
ENST00000324545.8:c.6365_6366del ENSP00000316357.6:p.Phe2122TyrfsTer22
ENST00000378308.6:c.6365_6366del ENSP00000367558.2:p.Phe2122TyrfsTer22
NM_001039590.2:c.6365_6366del NP_001034679.2:p.Phe2122TyrfsTer22
NM_001039591.2:c.6365_6366del NP_001034680.2:p.Phe2122TyrfsTer22
XM_005272675.3:c.6380_6381del XP_005272732.1:p.Phe2127TyrfsTer22
XM_005272676.3:c.6380_6381del XP_005272733.1:p.Phe2127TyrfsTer22
XM_005272675.4:c.6380_6381del XP_005272732.1:p.Phe2127TyrfsTer22
XM_005272676.4:c.6380_6381del XP_005272733.1:p.Phe2127TyrfsTer22
NM_001039591.3:c.6365_6366del MANE Select NP_001034680.2:p.Phe2122TyrfsTer22
NM_001039590.3:c.6365_6366del NP_001034679.2:p.Phe2122TyrfsTer22
Search 100 bp 5'
Search 100 bp 3'