Canonical Allele Identifier: CA1092300178

Gene: FBXL4

Linked Data

• dbSNP Id: rs1770623827
• gnomAD v3: 6-98875435-AACCTGGTAC-A
• gnomAD v4: 6-98875435-AACCTGGTAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875437_98875445del , CM000668.2:g.98875437_98875445del	GRCh38
NC_000006.11:g.99323313_99323321del , CM000668.1:g.99323313_99323321del	GRCh37
NC_000006.10:g.99430034_99430042del	NCBI36
NG_033903.1:g.77563_77571del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1673_1681del MANE Select	ENSP00000358247.1:p.Cys558_Arg560del
ENST00000229971.2:c.1673_1681del	ENSP00000229971.1:p.Cys558_Arg560del
ENST00000369244.6:c.1673_1681del	ENSP00000358247.1:p.Cys558_Arg560del
NM_001278716.1:c.1673_1681del	NP_001265645.1:p.Cys558_Arg560del
NM_012160.4:c.1673_1681del	NP_036292.2:p.Cys558_Arg560del
NR_103836.1:n.1718_1726del
XM_005266930.1:c.1601_1609del	XP_005266987.1:p.Cys534_Arg536del
XM_005266930.3:c.1601_1609del	XP_005266987.1:p.Cys534_Arg536del
XM_017010726.1:c.1673_1681del	XP_016866215.1:p.Cys558_Arg560del
XM_017010727.2:c.1601_1609del	XP_016866216.1:p.Cys534_Arg536del
XM_017010728.1:c.947_955del	XP_016866217.1:p.Cys316_Arg318del
NM_001278716.2:c.1673_1681del MANE Select	NP_001265645.1:p.Cys558_Arg560del
NR_103836.2:n.1658_1666del
NM_012160.5:c.1673_1681del	NP_036292.2:p.Cys558_Arg560del