Canonical Allele Identifier: CA2656313296

Gene: FBXO7

Linked Data

• gnomAD v4: 22-32484276-T-TCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32484278_32484279insGCA , CM000684.2:g.32484278_32484279insGCA	GRCh38
NC_000022.10:g.32880265_32880266insGCA , CM000684.1:g.32880265_32880266insGCA	GRCh37
NC_000022.9:g.31210265_31210266insGCA	NCBI36
NG_016001.1:g.14559_14560insGCA
NG_016001.2:g.14559_14560insGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.645+154_645+155insGCA MANE Select	ENSP00000266087.7:n.645+154_645+155insGCA
ENST00000266087.11:c.645+154_645+155insGCA	ENSP00000266087.7:n.645+154_645+155insGCA
ENST00000397426.5:c.303+154_303+155insGCA	ENSP00000380571.1:n.303+154_303+155insGCA
ENST00000420700.5:c.*224+154_*224+155insGCA	ENSP00000406155.1:n.*224+154_*224+155insGCA
ENST00000425028.5:c.*343+154_*343+155insGCA	ENSP00000395823.1:n.*343+154_*343+155insGCA
ENST00000452138.3:c.408+154_408+155insGCA	ENSP00000388547.2:n.408+154_408+155insGCA
ENST00000492535.1:n.481+154_481+155insGCA
NM_001033024.1:c.408+154_408+155insGCA	NP_001028196.1:n.408+154_408+155insGCA
NM_001257990.1:c.303+154_303+155insGCA	NP_001244919.1:n.303+154_303+155insGCA
NM_012179.3:c.645+154_645+155insGCA	NP_036311.3:n.645+154_645+155insGCA
XM_011530106.1:c.177+154_177+155insGCA	XP_011528408.1:n.177+154_177+155insGCA
XM_024452207.1:c.303+154_303+155insGCA	XP_024307975.1:n.303+154_303+155insGCA
NM_012179.4:c.645+154_645+155insGCA MANE Select	NP_036311.3:n.645+154_645+155insGCA
NM_001033024.2:c.408+154_408+155insGCA	NP_001028196.1:n.408+154_408+155insGCA
NM_001257990.2:c.303+154_303+155insGCA	NP_001244919.1:n.303+154_303+155insGCA