Canonical Allele Identifier: CA2573055305

Gene: USP9X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41153024_41153027del , CM000685.2:g.41153024_41153027del	GRCh38
NC_000023.10:g.41012277_41012280del , CM000685.1:g.41012277_41012280del	GRCh37
NC_000023.9:g.40897221_40897224del	NCBI36
NG_012547.1:g.72390_72393del

Transcript Alleles

HGVS	Amino-acid Change
NM_001039591.3:c.1840_1843del MANE Select	NP_001034680.2:p.Thr614TrpfsTer2
ENST00000378308.7:c.1840_1843del MANE Select	ENSP00000367558.2:p.Thr614TrpfsTer2
NM_001039590.2:c.1840_1843del	NP_001034679.2:p.Thr614TrpfsTer2
NM_001039590.3:c.1840_1843del	NP_001034679.2:p.Thr614TrpfsTer2
NM_001039591.2:c.1840_1843del	NP_001034680.2:p.Thr614TrpfsTer2
ENST00000324545.8:c.1840_1843del	ENSP00000316357.6:p.Thr614TrpfsTer2
ENST00000324545.9:c.1840_1843del	ENSP00000316357.6:p.Thr614TrpfsTer2
ENST00000378308.6:c.1840_1843del	ENSP00000367558.2:p.Thr614TrpfsTer2
ENST00000703986.1:c.1855_1858del	ENSP00000515603.1:p.Thr619TrpfsTer2
ENST00000703987.1:c.1855_1858del	ENSP00000515604.1:p.Thr619TrpfsTer2
ENST00000704649.1:c.1840_1843del	ENSP00000515974.1:p.Thr614TrpfsTer2
ENST00000704650.1:c.1840_1843del	ENSP00000515975.1:p.Thr614TrpfsTer2
ENST00000704651.1:c.1687_1690del	ENSP00000515976.1:p.Thr563TrpfsTer2
ENST00000704652.1:c.1070_1073del
ENST00000704653.1:c.320_323del	ENSP00000515978.1:n.320_323del
XM_005272675.3:c.1855_1858del	XP_005272732.1:p.Thr619TrpfsTer2
XM_005272675.4:c.1855_1858del	XP_005272732.1:p.Thr619TrpfsTer2
XM_005272676.3:c.1855_1858del	XP_005272733.1:p.Thr619TrpfsTer2
XM_005272676.4:c.1855_1858del	XP_005272733.1:p.Thr619TrpfsTer2