Canonical Allele Identifier: CA2401985171
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474979C= , CM000684.2:g.32474979C= GRCh38
NC_000022.10:g.32870966C= , CM000684.1:g.32870966C= GRCh37
NC_000022.9:g.31200966C= NCBI36
NG_016001.1:g.5260C=
NG_016001.2:g.5260C=

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-24C= MANE Select ENSP00000266087.7:n.-24C=
ENST00000266087.11:c.-24C= ENSP00000266087.7:n.-24C=
ENST00000420700.5:c.-24C= ENSP00000406155.1:n.-24C=
ENST00000425028.5:c.-24C= ENSP00000395823.1:n.-24C=
NM_012179.3:c.-24C= NP_036311.3:n.-24C=
XM_011530106.1:c.-197C= XP_011528408.1:n.-197C=
XM_024452207.1:c.-214C= XP_024307975.1:n.-214C=
NM_012179.4:c.-24C= MANE Select NP_036311.3:n.-24C=