Canonical Allele Identifier: CA920358700
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs1601499414

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474969del , CM000684.2:g.32474969del GRCh38
NC_000022.10:g.32870956del , CM000684.1:g.32870956del GRCh37
NC_000022.9:g.31200956del NCBI36
NG_016001.1:g.5250del
NG_016001.2:g.5250del

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-34del MANE Select ENSP00000266087.7:n.-34del
ENST00000266087.11:c.-34del ENSP00000266087.7:n.-34del
ENST00000420700.5:c.-34del ENSP00000406155.1:n.-34del
ENST00000425028.5:c.-34del ENSP00000395823.1:n.-34del
NM_012179.3:c.-34del NP_036311.3:n.-34del
XM_011530106.1:c.-207del XP_011528408.1:n.-207del
XM_024452207.1:c.-224del XP_024307975.1:n.-224del
NM_012179.4:c.-34del MANE Select NP_036311.3:n.-34del