Canonical Allele Identifier: CA2401985200
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475025T= , CM000684.2:g.32475025T= GRCh38
NC_000022.10:g.32871012T= , CM000684.1:g.32871012T= GRCh37
NC_000022.9:g.31201012T= NCBI36
NG_016001.1:g.5306T=
NG_016001.2:g.5306T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.23T= MANE Select ENSP00000266087.7:p.Leu8=
ENST00000266087.11:c.23T= ENSP00000266087.7:p.Leu8=
ENST00000420700.5:c.23T= ENSP00000406155.1:p.Leu8=
ENST00000425028.5:c.23T= ENSP00000395823.1:p.Leu8=
ENST00000492535.1:n.11T=
NM_012179.3:c.23T= NP_036311.3:p.Leu8=
XM_011530106.1:c.-151T= XP_011528408.1:n.-151T=
XM_024452207.1:c.-168T= XP_024307975.1:n.-168T=
NM_012179.4:c.23T= MANE Select NP_036311.3:p.Leu8=