Canonical Allele Identifier: CA2577697965

Gene: FBXO7

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32498125_32498128del , CM000684.2:g.32498125_32498128del	GRCh38
NC_000022.10:g.32894112_32894115del , CM000684.1:g.32894112_32894115del	GRCh37
NC_000022.9:g.31224112_31224115del	NCBI36
NG_016001.1:g.28406_28409del
NG_016001.2:g.28406_28409del

Transcript Alleles

HGVS	Amino-acid Change
NM_012179.4:c.1183-19_1183-16del MANE Select	NP_036311.3:n.1183-19_1183-16del
ENST00000266087.12:c.1183-19_1183-16del MANE Select	ENSP00000266087.7:n.1183-19_1183-16del
NM_001033024.1:c.946-19_946-16del	NP_001028196.1:n.946-19_946-16del
NM_001033024.2:c.946-19_946-16del	NP_001028196.1:n.946-19_946-16del
NM_001257990.1:c.841-19_841-16del	NP_001244919.1:n.841-19_841-16del
NM_001257990.2:c.841-19_841-16del	NP_001244919.1:n.841-19_841-16del
NM_012179.3:c.1183-19_1183-16del	NP_036311.3:n.1183-19_1183-16del
ENST00000266087.11:c.1183-19_1183-16del	ENSP00000266087.7:n.1183-19_1183-16del
ENST00000397426.5:c.841-19_841-16del	ENSP00000380571.1:n.841-19_841-16del
ENST00000420700.5:c.*762-19_*762-16del	ENSP00000406155.1:n.*762-19_*762-16del
ENST00000425028.5:c.*881-19_*881-16del	ENSP00000395823.1:n.*881-19_*881-16del
ENST00000452138.3:c.946-19_946-16del	ENSP00000388547.2:n.946-19_946-16del
ENST00000492535.1:n.6199-19_6199-16del
XM_011530106.1:c.715-19_715-16del	XP_011528408.1:n.715-19_715-16del
XM_024452207.1:c.841-19_841-16del	XP_024307975.1:n.841-19_841-16del