Canonical Allele Identifier: CA752552591

Gene: FBXO7

Linked Data

• dbSNP Id: rs1198934645
• gnomAD v3: 22-32484526-AC-A
• gnomAD v4: 22-32484526-AC-A
• MyVariant Identifiers: chr22:g.32880514del (hg19) ; chr22:g.32484527del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32484528del , CM000684.2:g.32484528del	GRCh38
NC_000022.10:g.32880515del , CM000684.1:g.32880515del	GRCh37
NC_000022.9:g.31210515del	NCBI36
NG_016001.1:g.14809del
NG_016001.2:g.14809del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.645+404del MANE Select	ENSP00000266087.7:n.645+404del
ENST00000266087.11:c.645+404del	ENSP00000266087.7:n.645+404del
ENST00000397426.5:c.303+404del	ENSP00000380571.1:n.303+404del
ENST00000420700.5:c.*224+404del	ENSP00000406155.1:n.*224+404del
ENST00000425028.5:c.*343+404del	ENSP00000395823.1:n.*343+404del
ENST00000452138.3:c.408+404del	ENSP00000388547.2:n.408+404del
ENST00000492535.1:n.481+404del
NM_001033024.1:c.408+404del	NP_001028196.1:n.408+404del
NM_001257990.1:c.303+404del	NP_001244919.1:n.303+404del
NM_012179.3:c.645+404del	NP_036311.3:n.645+404del
XM_011530106.1:c.177+404del	XP_011528408.1:n.177+404del
XM_024452207.1:c.303+404del	XP_024307975.1:n.303+404del
NM_012179.4:c.645+404del MANE Select	NP_036311.3:n.645+404del
NM_001033024.2:c.408+404del	NP_001028196.1:n.408+404del
NM_001257990.2:c.303+404del	NP_001244919.1:n.303+404del