Canonical Allele Identifier: CA2656311486

Gene: FBXO7

Linked Data

• gnomAD v4: 22-32475131-T-TGGGGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32475137_32475142dup , CM000684.2:g.32475137_32475142dup	GRCh38
NC_000022.10:g.32871124_32871129dup , CM000684.1:g.32871124_32871129dup	GRCh37
NC_000022.9:g.31201124_31201129dup	NCBI36
NG_016001.1:g.5418_5423dup
NG_016001.2:g.5418_5423dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.122+13_122+18dup MANE Select	ENSP00000266087.7:n.122+13_122+18dup
ENST00000266087.11:c.122+13_122+18dup	ENSP00000266087.7:n.122+13_122+18dup
ENST00000420700.5:c.122+13_122+18dup	ENSP00000406155.1:n.122+13_122+18dup
ENST00000425028.5:c.122+13_122+18dup	ENSP00000395823.1:n.122+13_122+18dup
ENST00000492535.1:n.110+13_110+18dup
NM_012179.3:c.122+13_122+18dup	NP_036311.3:n.122+13_122+18dup
XM_011530106.1:c.-52+13_-52+18dup	XP_011528408.1:n.-52+13_-52+18dup
XM_024452207.1:c.-69+13_-69+18dup	XP_024307975.1:n.-69+13_-69+18dup
NM_012179.4:c.122+13_122+18dup MANE Select	NP_036311.3:n.122+13_122+18dup