Canonical Allele Identifier: CA2679757634

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98875122-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875122_98875123insA , CM000668.2:g.98875122_98875123insA	GRCh38
NC_000006.11:g.99322998_99322999insA , CM000668.1:g.99322998_99322999insA	GRCh37
NC_000006.10:g.99429719_99429720insA	NCBI36
NG_033903.1:g.77884_77885insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+292_1702+293insT MANE Select	ENSP00000358247.1:n.1702+292_1702+293insT
ENST00000229971.2:c.1702+292_1702+293insT	ENSP00000229971.1:n.1702+292_1702+293insT
ENST00000369244.6:c.1702+292_1702+293insT	ENSP00000358247.1:n.1702+292_1702+293insT
NM_001278716.1:c.1702+292_1702+293insT	NP_001265645.1:n.1702+292_1702+293insT
NM_012160.4:c.1702+292_1702+293insT	NP_036292.2:n.1702+292_1702+293insT
NR_103836.1:n.1747+292_1747+293insT
XM_005266930.1:c.1630+292_1630+293insT	XP_005266987.1:n.1630+292_1630+293insT
XM_005266930.3:c.1630+292_1630+293insT	XP_005266987.1:n.1630+292_1630+293insT
XM_017010726.1:c.1702+292_1702+293insT	XP_016866215.1:n.1702+292_1702+293insT
XM_017010727.2:c.1630+292_1630+293insT	XP_016866216.1:n.1630+292_1630+293insT
XM_017010728.1:c.976+292_976+293insT	XP_016866217.1:n.976+292_976+293insT
NM_001278716.2:c.1702+292_1702+293insT MANE Select	NP_001265645.1:n.1702+292_1702+293insT
NR_103836.2:n.1687+292_1687+293insT
NM_012160.5:c.1702+292_1702+293insT	NP_036292.2:n.1702+292_1702+293insT