Canonical Allele Identifier: CA10201495

Gene: FBXO7

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32485097G>A , CM000684.2:g.32485097G>A	GRCh38
NC_000022.10:g.32881084G>A , CM000684.1:g.32881084G>A	GRCh37
NC_000022.9:g.31211084G>A	NCBI36
NG_016001.1:g.15378G>A
NG_016001.2:g.15378G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_012179.4:c.675G>A MANE Select	NP_036311.3:p.Pro225=
ENST00000266087.12:c.675G>A MANE Select	ENSP00000266087.7:p.Pro225=
NM_001033024.1:c.438G>A	NP_001028196.1:p.Pro146=
NM_001033024.2:c.438G>A	NP_001028196.1:p.Pro146=
NM_001257990.1:c.333G>A	NP_001244919.1:p.Pro111=
NM_001257990.2:c.333G>A	NP_001244919.1:p.Pro111=
NM_012179.3:c.675G>A	NP_036311.3:p.Pro225=
ENST00000266087.11:c.675G>A	ENSP00000266087.7:p.Pro225=
ENST00000397426.5:c.333G>A	ENSP00000380571.1:p.Pro111=
ENST00000420700.5:c.*254G>A	ENSP00000406155.1:n.*254G>A
ENST00000425028.5:c.*373G>A	ENSP00000395823.1:n.*373G>A
ENST00000452138.3:c.438G>A	ENSP00000388547.2:p.Pro146=
ENST00000492535.1:n.511G>A
XM_011530106.1:c.207G>A	XP_011528408.1:p.Pro69=
XM_024452207.1:c.333G>A	XP_024307975.1:p.Pro111=