Canonical Allele Identifier: CA2656311625

Gene: FBXO7

Linked Data

• gnomAD v4: 22-32475246-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32475250del , CM000684.2:g.32475250del	GRCh38
NC_000022.10:g.32871237del , CM000684.1:g.32871237del	GRCh37
NC_000022.9:g.31201237del	NCBI36
NG_016001.1:g.5531del
NG_016001.2:g.5531del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.122+126del MANE Select	ENSP00000266087.7:n.122+126del
ENST00000266087.11:c.122+126del	ENSP00000266087.7:n.122+126del
ENST00000420700.5:c.122+126del	ENSP00000406155.1:n.122+126del
ENST00000425028.5:c.122+126del	ENSP00000395823.1:n.122+126del
ENST00000452138.3:c.-112del	ENSP00000388547.2:n.-112del
ENST00000492535.1:n.110+126del
NM_001033024.1:c.-112del	NP_001028196.1:n.-112del
NM_001257990.1:c.-369del	NP_001244919.1:n.-369del
NM_012179.3:c.122+126del	NP_036311.3:n.122+126del
XM_011530106.1:c.-52+126del	XP_011528408.1:n.-52+126del
XM_024452207.1:c.-69+126del	XP_024307975.1:n.-69+126del
NM_012179.4:c.122+126del MANE Select	NP_036311.3:n.122+126del