Canonical Allele Identifier: CA2656311631

Gene: FBXO7

Linked Data

• gnomAD v4: 22-32475249-G-T

Genomic Alleles

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

Transcript Alleles

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