Canonical Allele Identifier: CA2496064477

Gene: FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47822948_47822954delinsGAAAAAT , CM000664.2:g.47822948_47822954delinsGAAAAAT	GRCh38
NC_000002.11:g.48050087_48050093delinsGAAAAAT , CM000664.1:g.48050087_48050093delinsGAAAAAT	GRCh37
NC_000002.10:g.47903591_47903597delinsGAAAAAT	NCBI36
NG_008397.1:g.87722_87728delinsATTTTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000681999.1:n.1493+189_1493+195delinsATTTTTC
ENST00000682451.1:n.1462+189_1462+195delinsATTTTTC
ENST00000682975.1:n.1511+189_1511+195delinsATTTTTC
ENST00000683894.1:c.1364+189_1364+195delinsATTTTTC	ENSP00000507789.1:n.1364+189_1364+195delinsATTTTTC
ENST00000684085.1:n.1493+189_1493+195delinsATTTTTC
ENST00000684712.1:n.1724+189_1724+195delinsATTTTTC
ENST00000403359.8:c.1616+189_1616+195delinsATTTTTC MANE Select	ENSP00000384823.4:n.1616+189_1616+195delinsATTTTTC
ENST00000316377.8:c.1382+189_1382+195delinsATTTTTC	ENSP00000323822.5:n.1382+189_1382+195delinsATTTTTC
ENST00000402508.5:c.1364+189_1364+195delinsATTTTTC	ENSP00000385398.1:n.1364+189_1364+195delinsATTTTTC
ENST00000403359.7:c.1616+189_1616+195delinsATTTTTC	ENSP00000384823.3:n.1616+189_1616+195delinsATTTTTC
ENST00000492225.5:n.1464+189_1464+195delinsATTTTTC
ENST00000493962.6:c.990+189_990+195delinsATTTTTC
NM_001190274.1:c.1616+189_1616+195delinsATTTTTC	NP_001177203.1:n.1616+189_1616+195delinsATTTTTC
NM_025133.4:c.1364+189_1364+195delinsATTTTTC	NP_079409.3:n.1364+189_1364+195delinsATTTTTC
XM_005264572.3:c.1616+189_1616+195delinsATTTTTC	XP_005264629.1:n.1616+189_1616+195delinsATTTTTC
XM_005264573.3:c.1613+189_1613+195delinsATTTTTC	XP_005264630.1:n.1613+189_1613+195delinsATTTTTC
XM_005264572.5:c.1616+189_1616+195delinsATTTTTC	XP_005264629.1:n.1616+189_1616+195delinsATTTTTC
XM_005264573.5:c.1613+189_1613+195delinsATTTTTC	XP_005264630.1:n.1613+189_1613+195delinsATTTTTC
XM_017005015.1:c.1613+189_1613+195delinsATTTTTC	XP_016860504.1:n.1613+189_1613+195delinsATTTTTC
XM_017005016.2:c.1364+189_1364+195delinsATTTTTC	XP_016860505.1:n.1364+189_1364+195delinsATTTTTC
XM_017005017.1:c.1364+189_1364+195delinsATTTTTC	XP_016860506.1:n.1364+189_1364+195delinsATTTTTC
NM_001190274.2:c.1616+189_1616+195delinsATTTTTC MANE Select	NP_001177203.1:n.1616+189_1616+195delinsATTTTTC
NM_001374325.1:c.1364+189_1364+195delinsATTTTTC	NP_001361254.1:n.1364+189_1364+195delinsATTTTTC