Canonical Allele Identifier: CA2496064502

Gene: FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47822993_47823009delinsATTCAGATGCACAGACT , CM000664.2:g.47822993_47823009delinsATTCAGATGCACAGACT	GRCh38
NC_000002.11:g.48050132_48050148delinsATTCAGATGCACAGACT , CM000664.1:g.48050132_48050148delinsATTCAGATGCACAGACT	GRCh37
NC_000002.10:g.47903636_47903652delinsATTCAGATGCACAGACT	NCBI36
NG_008397.1:g.87667_87683delinsAGTCTGTGCATCTGAAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000681999.1:n.1493+134_1493+150delinsAGTCTGTGCATCTGAAT
ENST00000682451.1:n.1462+134_1462+150delinsAGTCTGTGCATCTGAAT
ENST00000682975.1:n.1511+134_1511+150delinsAGTCTGTGCATCTGAAT
ENST00000683894.1:c.1364+134_1364+150delinsAGTCTGTGCATCTGAAT	ENSP00000507789.1:n.1364+134_1364+150delinsAGTCTGTGCATCTGAAT
ENST00000684085.1:n.1493+134_1493+150delinsAGTCTGTGCATCTGAAT
ENST00000684712.1:n.1724+134_1724+150delinsAGTCTGTGCATCTGAAT
ENST00000403359.8:c.1616+134_1616+150delinsAGTCTGTGCATCTGAAT MANE Select	ENSP00000384823.4:n.1616+134_1616+150delinsAGTCTGTGCATCTGAAT
ENST00000316377.8:c.1382+134_1382+150delinsAGTCTGTGCATCTGAAT	ENSP00000323822.5:n.1382+134_1382+150delinsAGTCTGTGCATCTGAAT
ENST00000402508.5:c.1364+134_1364+150delinsAGTCTGTGCATCTGAAT	ENSP00000385398.1:n.1364+134_1364+150delinsAGTCTGTGCATCTGAAT
ENST00000403359.7:c.1616+134_1616+150delinsAGTCTGTGCATCTGAAT	ENSP00000384823.3:n.1616+134_1616+150delinsAGTCTGTGCATCTGAAT
ENST00000492225.5:n.1464+134_1464+150delinsAGTCTGTGCATCTGAAT
ENST00000493962.6:c.990+134_990+150delinsAGTCTGTGCATCTGAAT
NM_001190274.1:c.1616+134_1616+150delinsAGTCTGTGCATCTGAAT	NP_001177203.1:n.1616+134_1616+150delinsAGTCTGTGCATCTGAAT
NM_025133.4:c.1364+134_1364+150delinsAGTCTGTGCATCTGAAT	NP_079409.3:n.1364+134_1364+150delinsAGTCTGTGCATCTGAAT
XM_005264572.3:c.1616+134_1616+150delinsAGTCTGTGCATCTGAAT	XP_005264629.1:n.1616+134_1616+150delinsAGTCTGTGCATCTGAAT
XM_005264573.3:c.1613+134_1613+150delinsAGTCTGTGCATCTGAAT	XP_005264630.1:n.1613+134_1613+150delinsAGTCTGTGCATCTGAAT
XM_005264572.5:c.1616+134_1616+150delinsAGTCTGTGCATCTGAAT	XP_005264629.1:n.1616+134_1616+150delinsAGTCTGTGCATCTGAAT
XM_005264573.5:c.1613+134_1613+150delinsAGTCTGTGCATCTGAAT	XP_005264630.1:n.1613+134_1613+150delinsAGTCTGTGCATCTGAAT
XM_017005015.1:c.1613+134_1613+150delinsAGTCTGTGCATCTGAAT	XP_016860504.1:n.1613+134_1613+150delinsAGTCTGTGCATCTGAAT
XM_017005016.2:c.1364+134_1364+150delinsAGTCTGTGCATCTGAAT	XP_016860505.1:n.1364+134_1364+150delinsAGTCTGTGCATCTGAAT
XM_017005017.1:c.1364+134_1364+150delinsAGTCTGTGCATCTGAAT	XP_016860506.1:n.1364+134_1364+150delinsAGTCTGTGCATCTGAAT
NM_001190274.2:c.1616+134_1616+150delinsAGTCTGTGCATCTGAAT MANE Select	NP_001177203.1:n.1616+134_1616+150delinsAGTCTGTGCATCTGAAT
NM_001374325.1:c.1364+134_1364+150delinsAGTCTGTGCATCTGAAT	NP_001361254.1:n.1364+134_1364+150delinsAGTCTGTGCATCTGAAT