Canonical Allele Identifier: CA411331703

Gene: FBXO7

Linked Data

• dbSNP Id: rs1458349518
• gnomAD v4: 22-32483999-T-A
• MyVariant Identifiers: chr22:g.32879986T>A (hg19) ; chr22:g.32483999T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32483999T>A , CM000684.2:g.32483999T>A	GRCh38
NC_000022.10:g.32879986T>A , CM000684.1:g.32879986T>A	GRCh37
NC_000022.9:g.31209986T>A	NCBI36
NG_016001.1:g.14280T>A
NG_016001.2:g.14280T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.520T>A MANE Select	ENSP00000266087.7:p.Ser174Thr
ENST00000266087.11:c.520T>A	ENSP00000266087.7:p.Ser174Thr
ENST00000397426.5:c.178T>A	ENSP00000380571.1:p.Ser60Thr
ENST00000420700.5:c.*99T>A	ENSP00000406155.1:n.*99T>A
ENST00000425028.5:c.*218T>A	ENSP00000395823.1:n.*218T>A
ENST00000452138.3:c.283T>A	ENSP00000388547.2:p.Ser95Thr
ENST00000492535.1:n.356T>A
NM_001033024.1:c.283T>A	NP_001028196.1:p.Ser95Thr
NM_001257990.1:c.178T>A	NP_001244919.1:p.Ser60Thr
NM_012179.3:c.520T>A	NP_036311.3:p.Ser174Thr
XM_011530106.1:c.52T>A	XP_011528408.1:p.Ser18Thr
XM_024452207.1:c.178T>A	XP_024307975.1:p.Ser60Thr
NM_012179.4:c.520T>A MANE Select	NP_036311.3:p.Ser174Thr
NM_001033024.2:c.283T>A	NP_001028196.1:p.Ser95Thr
NM_001257990.2:c.178T>A	NP_001244919.1:p.Ser60Thr