Canonical Allele Identifier: CA2401985174
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474981C= , CM000684.2:g.32474981C= GRCh38
NC_000022.10:g.32870968C= , CM000684.1:g.32870968C= GRCh37
NC_000022.9:g.31200968C= NCBI36
NG_016001.1:g.5262C=
NG_016001.2:g.5262C=

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-22C= MANE Select ENSP00000266087.7:n.-22C=
ENST00000266087.11:c.-22C= ENSP00000266087.7:n.-22C=
ENST00000420700.5:c.-22C= ENSP00000406155.1:n.-22C=
ENST00000425028.5:c.-22C= ENSP00000395823.1:n.-22C=
NM_012179.3:c.-22C= NP_036311.3:n.-22C=
XM_011530106.1:c.-195C= XP_011528408.1:n.-195C=
XM_024452207.1:c.-212C= XP_024307975.1:n.-212C=
NM_012179.4:c.-22C= MANE Select NP_036311.3:n.-22C=