Canonical Allele Identifier: CA2401985205
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475033A= , CM000684.2:g.32475033A= GRCh38
NC_000022.10:g.32871020A= , CM000684.1:g.32871020A= GRCh37
NC_000022.9:g.31201020A= NCBI36
NG_016001.1:g.5314A=
NG_016001.2:g.5314A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.31A= MANE Select ENSP00000266087.7:p.Thr11=
ENST00000266087.11:c.31A= ENSP00000266087.7:p.Thr11=
ENST00000420700.5:c.31A= ENSP00000406155.1:p.Thr11=
ENST00000425028.5:c.31A= ENSP00000395823.1:p.Thr11=
ENST00000492535.1:n.19A=
NM_012179.3:c.31A= NP_036311.3:p.Thr11=
XM_011530106.1:c.-143A= XP_011528408.1:n.-143A=
XM_024452207.1:c.-160A= XP_024307975.1:n.-160A=
NM_012179.4:c.31A= MANE Select NP_036311.3:p.Thr11=