Canonical Allele Identifier: CA2679757635

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98875123-CGCAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875124_98875127del , CM000668.2:g.98875124_98875127del	GRCh38
NC_000006.11:g.99323000_99323003del , CM000668.1:g.99323000_99323003del	GRCh37
NC_000006.10:g.99429721_99429724del	NCBI36
NG_033903.1:g.77880_77883del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+288_1702+291del MANE Select	ENSP00000358247.1:n.1702+288_1702+291del
ENST00000229971.2:c.1702+288_1702+291del	ENSP00000229971.1:n.1702+288_1702+291del
ENST00000369244.6:c.1702+288_1702+291del	ENSP00000358247.1:n.1702+288_1702+291del
NM_001278716.1:c.1702+288_1702+291del	NP_001265645.1:n.1702+288_1702+291del
NM_012160.4:c.1702+288_1702+291del	NP_036292.2:n.1702+288_1702+291del
NR_103836.1:n.1747+288_1747+291del
XM_005266930.1:c.1630+288_1630+291del	XP_005266987.1:n.1630+288_1630+291del
XM_005266930.3:c.1630+288_1630+291del	XP_005266987.1:n.1630+288_1630+291del
XM_017010726.1:c.1702+288_1702+291del	XP_016866215.1:n.1702+288_1702+291del
XM_017010727.2:c.1630+288_1630+291del	XP_016866216.1:n.1630+288_1630+291del
XM_017010728.1:c.976+288_976+291del	XP_016866217.1:n.976+288_976+291del
NM_001278716.2:c.1702+288_1702+291del MANE Select	NP_001265645.1:n.1702+288_1702+291del
NR_103836.2:n.1687+288_1687+291del
NM_012160.5:c.1702+288_1702+291del	NP_036292.2:n.1702+288_1702+291del