Canonical Allele Identifier: CA2679757616

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98875114-AAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875116_98875117del , CM000668.2:g.98875116_98875117del	GRCh38
NC_000006.11:g.99322992_99322993del , CM000668.1:g.99322992_99322993del	GRCh37
NC_000006.10:g.99429713_99429714del	NCBI36
NG_033903.1:g.77891_77892del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+299_1702+300del MANE Select	ENSP00000358247.1:n.1702+299_1702+300del
ENST00000229971.2:c.1702+299_1702+300del	ENSP00000229971.1:n.1702+299_1702+300del
ENST00000369244.6:c.1702+299_1702+300del	ENSP00000358247.1:n.1702+299_1702+300del
NM_001278716.1:c.1702+299_1702+300del	NP_001265645.1:n.1702+299_1702+300del
NM_012160.4:c.1702+299_1702+300del	NP_036292.2:n.1702+299_1702+300del
NR_103836.1:n.1747+299_1747+300del
XM_005266930.1:c.1630+299_1630+300del	XP_005266987.1:n.1630+299_1630+300del
XM_005266930.3:c.1630+299_1630+300del	XP_005266987.1:n.1630+299_1630+300del
XM_017010726.1:c.1702+299_1702+300del	XP_016866215.1:n.1702+299_1702+300del
XM_017010727.2:c.1630+299_1630+300del	XP_016866216.1:n.1630+299_1630+300del
XM_017010728.1:c.976+299_976+300del	XP_016866217.1:n.976+299_976+300del
NM_001278716.2:c.1702+299_1702+300del MANE Select	NP_001265645.1:n.1702+299_1702+300del
NR_103836.2:n.1687+299_1687+300del
NM_012160.5:c.1702+299_1702+300del	NP_036292.2:n.1702+299_1702+300del