Canonical Allele Identifier: CA645509409

Gene: USP9X

Linked Data

• ClinVar Variation Id: 438307
• ClinVar RCV Id: RCV000505256
• dbSNP Id: rs1555933969
• MyVariant Identifiers: chrX:g.41075415del (hg19) ; chrX:g.41216162del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41216162del , CM000685.2:g.41216162del	GRCh38
NC_000023.10:g.41075415del , CM000685.1:g.41075415del	GRCh37
NC_000023.9:g.40960359del	NCBI36
NG_012547.1:g.135528del

Transcript Alleles

HGVS	Amino-acid change
ENST00000703986.1:c.5610del	ENSP00000515603.1:p.Val1871TrpfsTer?
ENST00000703987.1:c.5610del	ENSP00000515604.1:p.Val1871TrpfsTer?
ENST00000704649.1:c.3685-16225del	ENSP00000515974.1:n.3685-16225del
ENST00000704650.1:c.5595del	ENSP00000515975.1:p.Val1866TrpfsTer?
ENST00000704651.1:c.5442del	ENSP00000515976.1:p.Val1815TrpfsTer?
ENST00000704652.1:c.4694del
ENST00000704654.1:c.2549del
ENST00000704655.1:c.1738del	ENSP00000515980.1:n.1738del
ENST00000704656.1:c.1046del	ENSP00000515981.1:n.1046del
ENST00000324545.9:c.5595del	ENSP00000316357.6:p.Val1866TrpfsTer?
ENST00000378308.7:c.5595del MANE Select	ENSP00000367558.2:p.Val1866TrpfsTer?
ENST00000324545.8:c.5595del	ENSP00000316357.6:p.Val1866TrpfsTer?
ENST00000378308.6:c.5595del	ENSP00000367558.2:p.Val1866TrpfsTer?
NM_001039590.2:c.5595del	NP_001034679.2:p.Val1866TrpfsTer?
NM_001039591.2:c.5595del	NP_001034680.2:p.Val1866TrpfsTer?
XM_005272675.3:c.5610del	XP_005272732.1:p.Val1871TrpfsTer?
XM_005272676.3:c.5610del	XP_005272733.1:p.Val1871TrpfsTer?
XM_005272675.4:c.5610del	XP_005272732.1:p.Val1871TrpfsTer?
XM_005272676.4:c.5610del	XP_005272733.1:p.Val1871TrpfsTer?
NM_001039591.3:c.5595del MANE Select	NP_001034680.2:p.Val1866TrpfsTer?
NM_001039590.3:c.5595del	NP_001034679.2:p.Val1866TrpfsTer?