Canonical Allele Identifier: CA2656311622

Gene: FBXO7

Linked Data

• gnomAD v4: 22-32475245-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32475245G>C , CM000684.2:g.32475245G>C	GRCh38
NC_000022.10:g.32871232G>C , CM000684.1:g.32871232G>C	GRCh37
NC_000022.9:g.31201232G>C	NCBI36
NG_016001.1:g.5526G>C
NG_016001.2:g.5526G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.122+121G>C MANE Select	ENSP00000266087.7:n.122+121G>C
ENST00000266087.11:c.122+121G>C	ENSP00000266087.7:n.122+121G>C
ENST00000420700.5:c.122+121G>C	ENSP00000406155.1:n.122+121G>C
ENST00000425028.5:c.122+121G>C	ENSP00000395823.1:n.122+121G>C
ENST00000452138.3:c.-117G>C	ENSP00000388547.2:n.-117G>C
ENST00000492535.1:n.110+121G>C
NM_001033024.1:c.-117G>C	NP_001028196.1:n.-117G>C
NM_001257990.1:c.-374G>C	NP_001244919.1:n.-374G>C
NM_012179.3:c.122+121G>C	NP_036311.3:n.122+121G>C
XM_011530106.1:c.-52+121G>C	XP_011528408.1:n.-52+121G>C
XM_024452207.1:c.-69+121G>C	XP_024307975.1:n.-69+121G>C
NM_012179.4:c.122+121G>C MANE Select	NP_036311.3:n.122+121G>C