Canonical Allele Identifier: CA2656311630

Gene: FBXO7

Linked Data

• gnomAD v4: 22-32475249-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32475249G>A , CM000684.2:g.32475249G>A	GRCh38
NC_000022.10:g.32871236G>A , CM000684.1:g.32871236G>A	GRCh37
NC_000022.9:g.31201236G>A	NCBI36
NG_016001.1:g.5530G>A
NG_016001.2:g.5530G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.122+125G>A MANE Select	ENSP00000266087.7:n.122+125G>A
ENST00000266087.11:c.122+125G>A	ENSP00000266087.7:n.122+125G>A
ENST00000420700.5:c.122+125G>A	ENSP00000406155.1:n.122+125G>A
ENST00000425028.5:c.122+125G>A	ENSP00000395823.1:n.122+125G>A
ENST00000452138.3:c.-113G>A	ENSP00000388547.2:n.-113G>A
ENST00000492535.1:n.110+125G>A
NM_001033024.1:c.-113G>A	NP_001028196.1:n.-113G>A
NM_001257990.1:c.-370G>A	NP_001244919.1:n.-370G>A
NM_012179.3:c.122+125G>A	NP_036311.3:n.122+125G>A
XM_011530106.1:c.-52+125G>A	XP_011528408.1:n.-52+125G>A
XM_024452207.1:c.-69+125G>A	XP_024307975.1:n.-69+125G>A
NM_012179.4:c.122+125G>A MANE Select	NP_036311.3:n.122+125G>A