Canonical Allele Identifier: CA2679757759

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98875693-CCTATCATGCTAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875700_98875711del , CM000668.2:g.98875700_98875711del	GRCh38
NC_000006.11:g.99323576_99323587del , CM000668.1:g.99323576_99323587del	GRCh37
NC_000006.10:g.99430297_99430308del	NCBI36
NG_033903.1:g.77302_77313del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1412_1423del MANE Select	ENSP00000358247.1:p.Ala471_Ile474del
ENST00000229971.2:c.1412_1423del	ENSP00000229971.1:p.Ala471_Ile474del
ENST00000369244.6:c.1412_1423del	ENSP00000358247.1:p.Ala471_Ile474del
NM_001278716.1:c.1412_1423del	NP_001265645.1:p.Ala471_Ile474del
NM_012160.4:c.1412_1423del	NP_036292.2:p.Ala471_Ile474del
NR_103836.1:n.1457_1468del
XM_005266930.1:c.1340_1351del	XP_005266987.1:p.Ala447_Ile450del
XM_005266930.3:c.1340_1351del	XP_005266987.1:p.Ala447_Ile450del
XM_017010726.1:c.1412_1423del	XP_016866215.1:p.Ala471_Ile474del
XM_017010727.2:c.1340_1351del	XP_016866216.1:p.Ala447_Ile450del
XM_017010728.1:c.686_697del	XP_016866217.1:p.Ala229_Ile232del
NM_001278716.2:c.1412_1423del MANE Select	NP_001265645.1:p.Ala471_Ile474del
NR_103836.2:n.1397_1408del
NM_012160.5:c.1412_1423del	NP_036292.2:p.Ala471_Ile474del