Canonical Allele Identifier: CA2658973933

Gene: FBXO11

Linked Data

• gnomAD v4: 2-47839361-TCAAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47839365_47839368del , CM000664.2:g.47839365_47839368del	GRCh38
NC_000002.11:g.48066504_48066507del , CM000664.1:g.48066504_48066507del	GRCh37
NC_000002.10:g.47920008_47920011del	NCBI36
NG_008397.1:g.71311_71314del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681999.1:n.319+54_319+57del
ENST00000682451.1:n.291+54_291+57del
ENST00000682975.1:n.337+54_337+57del
ENST00000683894.1:c.190+54_190+57del	ENSP00000507789.1:n.190+54_190+57del
ENST00000684085.1:n.319+54_319+57del
ENST00000684712.1:n.550+54_550+57del
ENST00000403359.8:c.442+54_442+57del MANE Select	ENSP00000384823.4:n.442+54_442+57del
ENST00000316377.8:c.208+54_208+57del	ENSP00000323822.5:n.208+54_208+57del
ENST00000402508.5:c.190+54_190+57del	ENSP00000385398.1:n.190+54_190+57del
ENST00000403359.7:c.442+54_442+57del	ENSP00000384823.3:n.442+54_442+57del
ENST00000424163.2:c.190+54_190+57del	ENSP00000392272.1:n.190+54_190+57del
ENST00000480038.1:n.405+54_405+57del
ENST00000492225.5:n.290+54_290+57del
NM_001190274.1:c.442+54_442+57del	NP_001177203.1:n.442+54_442+57del
NM_025133.4:c.190+54_190+57del	NP_079409.3:n.190+54_190+57del
XM_005264572.3:c.442+54_442+57del	XP_005264629.1:n.442+54_442+57del
XM_005264573.3:c.442+54_442+57del	XP_005264630.1:n.442+54_442+57del
XM_005264572.5:c.442+54_442+57del	XP_005264629.1:n.442+54_442+57del
XM_005264573.5:c.442+54_442+57del	XP_005264630.1:n.442+54_442+57del
XM_017005015.1:c.442+54_442+57del	XP_016860504.1:n.442+54_442+57del
XM_017005016.2:c.190+54_190+57del	XP_016860505.1:n.190+54_190+57del
XM_017005017.1:c.190+54_190+57del	XP_016860506.1:n.190+54_190+57del
NM_001190274.2:c.442+54_442+57del MANE Select	NP_001177203.1:n.442+54_442+57del
NM_001374325.1:c.190+54_190+57del	NP_001361254.1:n.190+54_190+57del