Canonical Allele Identifier: CA2496064507

Gene: FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47823001_47823003delinsGCA , CM000664.2:g.47823001_47823003delinsGCA	GRCh38
NC_000002.11:g.48050140_48050142delinsGCA , CM000664.1:g.48050140_48050142delinsGCA	GRCh37
NC_000002.10:g.47903644_47903646delinsGCA	NCBI36
NG_008397.1:g.87673_87675delinsTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681999.1:n.1493+140_1493+142delinsTGC
ENST00000682451.1:n.1462+140_1462+142delinsTGC
ENST00000682975.1:n.1511+140_1511+142delinsTGC
ENST00000683894.1:c.1364+140_1364+142delinsTGC	ENSP00000507789.1:n.1364+140_1364+142delinsTGC
ENST00000684085.1:n.1493+140_1493+142delinsTGC
ENST00000684712.1:n.1724+140_1724+142delinsTGC
ENST00000403359.8:c.1616+140_1616+142delinsTGC MANE Select	ENSP00000384823.4:n.1616+140_1616+142delinsTGC
ENST00000316377.8:c.1382+140_1382+142delinsTGC	ENSP00000323822.5:n.1382+140_1382+142delinsTGC
ENST00000402508.5:c.1364+140_1364+142delinsTGC	ENSP00000385398.1:n.1364+140_1364+142delinsTGC
ENST00000403359.7:c.1616+140_1616+142delinsTGC	ENSP00000384823.3:n.1616+140_1616+142delinsTGC
ENST00000492225.5:n.1464+140_1464+142delinsTGC
ENST00000493962.6:c.990+140_990+142delinsTGC
NM_001190274.1:c.1616+140_1616+142delinsTGC	NP_001177203.1:n.1616+140_1616+142delinsTGC
NM_025133.4:c.1364+140_1364+142delinsTGC	NP_079409.3:n.1364+140_1364+142delinsTGC
XM_005264572.3:c.1616+140_1616+142delinsTGC	XP_005264629.1:n.1616+140_1616+142delinsTGC
XM_005264573.3:c.1613+140_1613+142delinsTGC	XP_005264630.1:n.1613+140_1613+142delinsTGC
XM_005264572.5:c.1616+140_1616+142delinsTGC	XP_005264629.1:n.1616+140_1616+142delinsTGC
XM_005264573.5:c.1613+140_1613+142delinsTGC	XP_005264630.1:n.1613+140_1613+142delinsTGC
XM_017005015.1:c.1613+140_1613+142delinsTGC	XP_016860504.1:n.1613+140_1613+142delinsTGC
XM_017005016.2:c.1364+140_1364+142delinsTGC	XP_016860505.1:n.1364+140_1364+142delinsTGC
XM_017005017.1:c.1364+140_1364+142delinsTGC	XP_016860506.1:n.1364+140_1364+142delinsTGC
NM_001190274.2:c.1616+140_1616+142delinsTGC MANE Select	NP_001177203.1:n.1616+140_1616+142delinsTGC
NM_001374325.1:c.1364+140_1364+142delinsTGC	NP_001361254.1:n.1364+140_1364+142delinsTGC