Canonical Allele Identifier: CA2401985168
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474974C= , CM000684.2:g.32474974C= GRCh38
NC_000022.10:g.32870961C= , CM000684.1:g.32870961C= GRCh37
NC_000022.9:g.31200961C= NCBI36
NG_016001.1:g.5255C=
NG_016001.2:g.5255C=

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-29C= MANE Select ENSP00000266087.7:n.-29C=
ENST00000266087.11:c.-29C= ENSP00000266087.7:n.-29C=
ENST00000420700.5:c.-29C= ENSP00000406155.1:n.-29C=
ENST00000425028.5:c.-29C= ENSP00000395823.1:n.-29C=
NM_012179.3:c.-29C= NP_036311.3:n.-29C=
XM_011530106.1:c.-202C= XP_011528408.1:n.-202C=
XM_024452207.1:c.-219C= XP_024307975.1:n.-219C=
NM_012179.4:c.-29C= MANE Select NP_036311.3:n.-29C=