Canonical Allele Identifier: CA16043637
Gene: USP9X HGNC NCBI

Linked Data

ClinVar Variation Id: 374246
ClinVar RCV Id: RCV000415029
dbSNP Id: rs1057519007
MyVariant Identifiers: chrX:g.41075159_41075160del (hg19) chrX:g.41215906_41215907del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41215906_41215907del , CM000685.2:g.41215906_41215907del GRCh38
NC_000023.10:g.41075159_41075160del , CM000685.1:g.41075159_41075160del GRCh37
NC_000023.9:g.40960103_40960104del NCBI36
NG_012547.1:g.135272_135273del

Transcript Alleles

HGVS Amino-acid change
ENST00000703986.1:c.5354_5355del ENSP00000515603.1:p.Thr1785SerfsTer7
ENST00000703987.1:c.5354_5355del ENSP00000515604.1:p.Thr1785SerfsTer7
ENST00000704649.1:c.3685-16481_3685-16480del ENSP00000515974.1:n.3685-16481_3685-16480...
ENST00000704650.1:c.5339_5340del ENSP00000515975.1:p.Thr1780SerfsTer7
ENST00000704651.1:c.5186_5187del ENSP00000515976.1:p.Thr1729SerfsTer7
ENST00000704652.1:c.4438_4439del
ENST00000704654.1:c.2293_2294del
ENST00000704655.1:c.1482_1483del ENSP00000515980.1:n.1482_1483del
ENST00000704656.1:c.790_791del ENSP00000515981.1:p.Pro264ValfsTer?
ENST00000324545.9:c.5339_5340del ENSP00000316357.6:p.Thr1780SerfsTer7
ENST00000378308.7:c.5339_5340del MANE Select ENSP00000367558.2:p.Thr1780SerfsTer7
ENST00000324545.8:c.5339_5340del ENSP00000316357.6:p.Thr1780SerfsTer7
ENST00000378308.6:c.5339_5340del ENSP00000367558.2:p.Thr1780SerfsTer7
NM_001039590.2:c.5339_5340del NP_001034679.2:p.Thr1780SerfsTer7
NM_001039591.2:c.5339_5340del NP_001034680.2:p.Thr1780SerfsTer7
XM_005272675.3:c.5354_5355del XP_005272732.1:p.Thr1785SerfsTer7
XM_005272676.3:c.5354_5355del XP_005272733.1:p.Thr1785SerfsTer7
XM_005272675.4:c.5354_5355del XP_005272732.1:p.Thr1785SerfsTer7
XM_005272676.4:c.5354_5355del XP_005272733.1:p.Thr1785SerfsTer7
NM_001039591.3:c.5339_5340del MANE Select NP_001034680.2:p.Thr1780SerfsTer7
NM_001039590.3:c.5339_5340del NP_001034679.2:p.Thr1780SerfsTer7
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