Canonical Allele Identifier: CA769481273
Gene: FBXO11 HGNC NCBI

Linked Data

dbSNP Id: rs1167692109

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47823004_47823005del , CM000664.2:g.47823004_47823005del GRCh38
NC_000002.11:g.48050143_48050144del , CM000664.1:g.48050143_48050144del GRCh37
NC_000002.10:g.47903647_47903648del NCBI36
NG_008397.1:g.87673_87674del

Transcript Alleles

HGVS Amino-acid change
ENST00000681999.1:n.1493+140_1493+141del
ENST00000682451.1:n.1462+140_1462+141del
ENST00000682975.1:n.1511+140_1511+141del
ENST00000683894.1:c.1364+140_1364+141del ENSP00000507789.1:n.1364+140_1364+141del
ENST00000684085.1:n.1493+140_1493+141del
ENST00000684712.1:n.1724+140_1724+141del
ENST00000403359.8:c.1616+140_1616+141del MANE Select ENSP00000384823.4:n.1616+140_1616+141del
ENST00000316377.8:c.1382+140_1382+141del ENSP00000323822.5:n.1382+140_1382+141del
ENST00000402508.5:c.1364+140_1364+141del ENSP00000385398.1:n.1364+140_1364+141del
ENST00000403359.7:c.1616+140_1616+141del ENSP00000384823.3:n.1616+140_1616+141del
ENST00000492225.5:n.1464+140_1464+141del
ENST00000493962.6:c.990+140_990+141del
NM_001190274.1:c.1616+140_1616+141del NP_001177203.1:n.1616+140_1616+141del
NM_025133.4:c.1364+140_1364+141del NP_079409.3:n.1364+140_1364+141del
XM_005264572.3:c.1616+140_1616+141del XP_005264629.1:n.1616+140_1616+141del
XM_005264573.3:c.1613+140_1613+141del XP_005264630.1:n.1613+140_1613+141del
XM_005264572.5:c.1616+140_1616+141del XP_005264629.1:n.1616+140_1616+141del
XM_005264573.5:c.1613+140_1613+141del XP_005264630.1:n.1613+140_1613+141del
XM_017005015.1:c.1613+140_1613+141del XP_016860504.1:n.1613+140_1613+141del
XM_017005016.2:c.1364+140_1364+141del XP_016860505.1:n.1364+140_1364+141del
XM_017005017.1:c.1364+140_1364+141del XP_016860506.1:n.1364+140_1364+141del
NM_001190274.2:c.1616+140_1616+141del MANE Select NP_001177203.1:n.1616+140_1616+141del
NM_001374325.1:c.1364+140_1364+141del NP_001361254.1:n.1364+140_1364+141del