Canonical Allele Identifier: CA2401985195
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475014G= , CM000684.2:g.32475014G= GRCh38
NC_000022.10:g.32871001G= , CM000684.1:g.32871001G= GRCh37
NC_000022.9:g.31201001G= NCBI36
NG_016001.1:g.5295G=
NG_016001.2:g.5295G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.12G= MANE Select ENSP00000266087.7:p.Arg4=
ENST00000266087.11:c.12G= ENSP00000266087.7:p.Arg4=
ENST00000420700.5:c.12G= ENSP00000406155.1:p.Arg4=
ENST00000425028.5:c.12G= ENSP00000395823.1:p.Arg4=
NM_012179.3:c.12G= NP_036311.3:p.Arg4=
XM_011530106.1:c.-162G= XP_011528408.1:n.-162G=
XM_024452207.1:c.-179G= XP_024307975.1:n.-179G=
NM_012179.4:c.12G= MANE Select NP_036311.3:p.Arg4=