Canonical Allele Identifier: CA752552597

Gene: FBXO7

Linked Data

• dbSNP Id: rs1247937791
• gnomAD v3: 22-32484543-TA-T
• gnomAD v4: 22-32484543-TA-T
• MyVariant Identifiers: chr22:g.32880531del (hg19) ; chr22:g.32484544del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32484548del , CM000684.2:g.32484548del	GRCh38
NC_000022.10:g.32880535del , CM000684.1:g.32880535del	GRCh37
NC_000022.9:g.31210535del	NCBI36
NG_016001.1:g.14829del
NG_016001.2:g.14829del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.645+424del MANE Select	ENSP00000266087.7:n.645+424del
ENST00000266087.11:c.645+424del	ENSP00000266087.7:n.645+424del
ENST00000397426.5:c.303+424del	ENSP00000380571.1:n.303+424del
ENST00000420700.5:c.*224+424del	ENSP00000406155.1:n.*224+424del
ENST00000425028.5:c.*343+424del	ENSP00000395823.1:n.*343+424del
ENST00000452138.3:c.408+424del	ENSP00000388547.2:n.408+424del
ENST00000492535.1:n.481+424del
NM_001033024.1:c.408+424del	NP_001028196.1:n.408+424del
NM_001257990.1:c.303+424del	NP_001244919.1:n.303+424del
NM_012179.3:c.645+424del	NP_036311.3:n.645+424del
XM_011530106.1:c.177+424del	XP_011528408.1:n.177+424del
XM_024452207.1:c.303+424del	XP_024307975.1:n.303+424del
NM_012179.4:c.645+424del MANE Select	NP_036311.3:n.645+424del
NM_001033024.2:c.408+424del	NP_001028196.1:n.408+424del
NM_001257990.2:c.303+424del	NP_001244919.1:n.303+424del