Canonical Allele Identifier: CA2656311482
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475131_32475136del , CM000684.2:g.32475131_32475136del GRCh38
NC_000022.10:g.32871118_32871123del , CM000684.1:g.32871118_32871123del GRCh37
NC_000022.9:g.31201118_31201123del NCBI36
NG_016001.1:g.5412_5417del
NG_016001.2:g.5412_5417del

Transcript Alleles

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