Canonical Allele Identifier: CA2496064476

Gene: FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47822948_47822970delinsGAAAAATAAAAACACCAAAAAAT , CM000664.2:g.47822948_47822970delinsGAAAAATAAAAACACCAAAAAAT	GRCh38
NC_000002.11:g.48050087_48050109delinsGAAAAATAAAAACACCAAAAAAT , CM000664.1:g.48050087_48050109delinsGAAAAATAAAAACACCAAAAAAT	GRCh37
NC_000002.10:g.47903591_47903613delinsGAAAAATAAAAACACCAAAAAAT	NCBI36
NG_008397.1:g.87706_87728delinsATTTTTTGGTGTTTTTATTTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681999.1:n.1493+173_1493+195delinsATTTTTTGGTGTTTTTATTTTTC
ENST00000682451.1:n.1462+173_1462+195delinsATTTTTTGGTGTTTTTATTTTTC
ENST00000682975.1:n.1511+173_1511+195delinsATTTTTTGGTGTTTTTATTTTTC
ENST00000683894.1:c.1364+173_1364+195delinsATTTTTTGGTGTTTTTATTTTTC	ENSP00000507789.1:n.1364+173_1364+195delinsATTTTTTGGTGTTTTTAT...
ENST00000684085.1:n.1493+173_1493+195delinsATTTTTTGGTGTTTTTATTTTTC
ENST00000684712.1:n.1724+173_1724+195delinsATTTTTTGGTGTTTTTATTTTTC
ENST00000403359.8:c.1616+173_1616+195delinsATTTTTTGGTGTTTTTATTTTTC MANE Select	ENSP00000384823.4:n.1616+173_1616+195delinsATTTTTTGGTGTTTTTAT...
ENST00000316377.8:c.1382+173_1382+195delinsATTTTTTGGTGTTTTTATTTTTC	ENSP00000323822.5:n.1382+173_1382+195delinsATTTTTTGGTGTTTTTAT...
ENST00000402508.5:c.1364+173_1364+195delinsATTTTTTGGTGTTTTTATTTTTC	ENSP00000385398.1:n.1364+173_1364+195delinsATTTTTTGGTGTTTTTAT...
ENST00000403359.7:c.1616+173_1616+195delinsATTTTTTGGTGTTTTTATTTTTC	ENSP00000384823.3:n.1616+173_1616+195delinsATTTTTTGGTGTTTTTAT...
ENST00000492225.5:n.1464+173_1464+195delinsATTTTTTGGTGTTTTTATTTTTC
ENST00000493962.6:c.990+173_990+195delinsATTTTTTGGTGTTTTTATTTTTC
NM_001190274.1:c.1616+173_1616+195delinsATTTTTTGGTGTTTTTATTTTTC	NP_001177203.1:n.1616+173_1616+195delinsATTTTTTGGTGTTTTTATTTT...
NM_025133.4:c.1364+173_1364+195delinsATTTTTTGGTGTTTTTATTTTTC	NP_079409.3:n.1364+173_1364+195delinsATTTTTTGGTGTTTTTATTTTTC
XM_005264572.3:c.1616+173_1616+195delinsATTTTTTGGTGTTTTTATTTTTC	XP_005264629.1:n.1616+173_1616+195delinsATTTTTTGGTGTTTTTATTTT...
XM_005264573.3:c.1613+173_1613+195delinsATTTTTTGGTGTTTTTATTTTTC	XP_005264630.1:n.1613+173_1613+195delinsATTTTTTGGTGTTTTTATTTT...
XM_005264572.5:c.1616+173_1616+195delinsATTTTTTGGTGTTTTTATTTTTC	XP_005264629.1:n.1616+173_1616+195delinsATTTTTTGGTGTTTTTATTTT...
XM_005264573.5:c.1613+173_1613+195delinsATTTTTTGGTGTTTTTATTTTTC	XP_005264630.1:n.1613+173_1613+195delinsATTTTTTGGTGTTTTTATTTT...
XM_017005015.1:c.1613+173_1613+195delinsATTTTTTGGTGTTTTTATTTTTC	XP_016860504.1:n.1613+173_1613+195delinsATTTTTTGGTGTTTTTATTTT...
XM_017005016.2:c.1364+173_1364+195delinsATTTTTTGGTGTTTTTATTTTTC	XP_016860505.1:n.1364+173_1364+195delinsATTTTTTGGTGTTTTTATTTT...
XM_017005017.1:c.1364+173_1364+195delinsATTTTTTGGTGTTTTTATTTTTC	XP_016860506.1:n.1364+173_1364+195delinsATTTTTTGGTGTTTTTATTTT...
NM_001190274.2:c.1616+173_1616+195delinsATTTTTTGGTGTTTTTATTTTTC MANE Select	NP_001177203.1:n.1616+173_1616+195delinsATTTTTTGGTGTTTTTATTTT...
NM_001374325.1:c.1364+173_1364+195delinsATTTTTTGGTGTTTTTATTTTTC	NP_001361254.1:n.1364+173_1364+195delinsATTTTTTGGTGTTTTTATTTT...