Canonical Allele Identifier: CA2401985142
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs2057415927

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474949del , CM000684.2:g.32474949del GRCh38
NC_000022.10:g.32870936del , CM000684.1:g.32870936del GRCh37
NC_000022.9:g.31200936del NCBI36
NG_016001.1:g.5230del
NG_016001.2:g.5230del

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-54del MANE Select ENSP00000266087.7:n.-54del
ENST00000266087.11:c.-54del ENSP00000266087.7:n.-54del
ENST00000420700.5:c.-54del ENSP00000406155.1:n.-54del
ENST00000425028.5:c.-54del ENSP00000395823.1:n.-54del
NM_012179.3:c.-54del NP_036311.3:n.-54del
XM_011530106.1:c.-227del XP_011528408.1:n.-227del
XM_024452207.1:c.-244del XP_024307975.1:n.-244del
NM_012179.4:c.-54del MANE Select NP_036311.3:n.-54del