Canonical Allele Identifier: CA1092299770

Gene: FBXL4

Linked Data

• dbSNP Id: rs1770569849
• gnomAD v3: 6-98874176-CTTAA-C
• gnomAD v4: 6-98874176-CTTAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874179_98874182del , CM000668.2:g.98874179_98874182del	GRCh38
NC_000006.11:g.99322055_99322058del , CM000668.1:g.99322055_99322058del	GRCh37
NC_000006.10:g.99428776_99428779del	NCBI36
NG_033903.1:g.78827_78830del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.*98_*101del MANE Select	ENSP00000358247.1:n.*98_*101del
ENST00000229971.2:c.*98_*101del	ENSP00000229971.1:n.*98_*101del
ENST00000369244.6:c.*98_*101del	ENSP00000358247.1:n.*98_*101del
NM_001278716.1:c.*98_*101del	NP_001265645.1:n.*98_*101del
NM_012160.4:c.*98_*101del	NP_036292.2:n.*98_*101del
NR_103836.1:n.2009_2012del
XM_005266930.1:c.*98_*101del	XP_005266987.1:n.*98_*101del
XM_005266930.3:c.*98_*101del	XP_005266987.1:n.*98_*101del
XM_017010726.1:c.*98_*101del	XP_016866215.1:n.*98_*101del
XM_017010727.2:c.*98_*101del	XP_016866216.1:n.*98_*101del
XM_017010728.1:c.*98_*101del	XP_016866217.1:n.*98_*101del
NM_001278716.2:c.*98_*101del MANE Select	NP_001265645.1:n.*98_*101del
NR_103836.2:n.1949_1952del
NM_012160.5:c.*98_*101del	NP_036292.2:n.*98_*101del