Canonical Allele Identifier: CA151370
Gene: USP9X HGNC NCBI

Linked Data

ClinVar Variation Id: 127091
ClinVar RCV Id: RCV000114950
dbSNP Id: rs587777318
MyVariant Identifiers: chrX:g.41089848del (hg19) chrX:g.41230595del (hg38)
PubMed: PMID:19377476 PMID:24607389
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41230595del , CM000685.2:g.41230595del GRCh38
NC_000023.10:g.41089848del , CM000685.1:g.41089848del GRCh37
NC_000023.9:g.40974792del NCBI36
NG_012547.1:g.149961del

Transcript Alleles

HGVS Amino-acid change
ENST00000703986.1:c.7541del ENSP00000515603.1:p.Gln2514ArgfsTer18
ENST00000703987.1:c.7589del ENSP00000515604.1:p.Gln2530ArgfsTer18
ENST00000704649.1:c.3685-1792del ENSP00000515974.1:n.3685-1792del
ENST00000704650.1:c.7526del ENSP00000515975.1:p.Gln2509ArgfsTer18
ENST00000704651.1:c.7373del ENSP00000515976.1:p.Gln2458ArgfsTer18
ENST00000704652.1:c.6625del
ENST00000704654.1:c.4405del
ENST00000704655.1:c.3669del ENSP00000515980.1:n.3669del
ENST00000704656.1:c.2977del ENSP00000515981.1:n.2977del
ENST00000324545.9:c.7574del ENSP00000316357.6:p.Gln2525ArgfsTer18
ENST00000378308.7:c.7526del MANE Select ENSP00000367558.2:p.Gln2509ArgfsTer18
ENST00000324545.8:c.7574del ENSP00000316357.6:p.Gln2525ArgfsTer18
ENST00000378308.6:c.7526del ENSP00000367558.2:p.Gln2509ArgfsTer18
NM_001039590.2:c.7574del NP_001034679.2:p.Gln2525ArgfsTer18
NM_001039591.2:c.7526del NP_001034680.2:p.Gln2509ArgfsTer18
XM_005272675.3:c.7589del XP_005272732.1:p.Gln2530ArgfsTer18
XM_005272676.3:c.7541del XP_005272733.1:p.Gln2514ArgfsTer18
XM_005272675.4:c.7589del XP_005272732.1:p.Gln2530ArgfsTer18
XM_005272676.4:c.7541del XP_005272733.1:p.Gln2514ArgfsTer18
NM_001039591.3:c.7526del MANE Select NP_001034680.2:p.Gln2509ArgfsTer18
NM_001039590.3:c.7574del NP_001034679.2:p.Gln2525ArgfsTer18
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