Canonical Allele Identifier: CA2679757534

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98874274-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874275_98874276del , CM000668.2:g.98874275_98874276del	GRCh38
NC_000006.11:g.99322151_99322152del , CM000668.1:g.99322151_99322152del	GRCh37
NC_000006.10:g.99428872_99428873del	NCBI36
NG_033903.1:g.78731_78732del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.*2_*3del MANE Select	ENSP00000358247.1:n.*2_*3del
ENST00000229971.2:c.*2_*3del	ENSP00000229971.1:n.*2_*3del
ENST00000369244.6:c.*2_*3del	ENSP00000358247.1:n.*2_*3del
NM_001278716.1:c.*2_*3del	NP_001265645.1:n.*2_*3del
NM_012160.4:c.*2_*3del	NP_036292.2:n.*2_*3del
NR_103836.1:n.1913_1914del
XM_005266930.1:c.*2_*3del	XP_005266987.1:n.*2_*3del
XM_005266930.3:c.*2_*3del	XP_005266987.1:n.*2_*3del
XM_017010726.1:c.*2_*3del	XP_016866215.1:n.*2_*3del
XM_017010727.2:c.*2_*3del	XP_016866216.1:n.*2_*3del
XM_017010728.1:c.*2_*3del	XP_016866217.1:n.*2_*3del
NM_001278716.2:c.*2_*3del MANE Select	NP_001265645.1:n.*2_*3del
NR_103836.2:n.1853_1854del
NM_012160.5:c.*2_*3del	NP_036292.2:n.*2_*3del