Canonical Allele Identifier: CA2401985150

Gene: FBXO7

Linked Data

• dbSNP Id: rs2057416032
• gnomAD v4: 22-32474955-CCCGTCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32474959_32474964del , CM000684.2:g.32474959_32474964del	GRCh38
NC_000022.10:g.32870946_32870951del , CM000684.1:g.32870946_32870951del	GRCh37
NC_000022.9:g.31200946_31200951del	NCBI36
NG_016001.1:g.5240_5245del
NG_016001.2:g.5240_5245del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.-44_-39del MANE Select	ENSP00000266087.7:n.-44_-39del
ENST00000266087.11:c.-44_-39del	ENSP00000266087.7:n.-44_-39del
ENST00000420700.5:c.-44_-39del	ENSP00000406155.1:n.-44_-39del
ENST00000425028.5:c.-44_-39del	ENSP00000395823.1:n.-44_-39del
NM_012179.3:c.-44_-39del	NP_036311.3:n.-44_-39del
XM_011530106.1:c.-217_-212del	XP_011528408.1:n.-217_-212del
XM_024452207.1:c.-234_-229del	XP_024307975.1:n.-234_-229del
NM_012179.4:c.-44_-39del MANE Select	NP_036311.3:n.-44_-39del