Canonical Allele Identifier: CA2401985207
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475035C= , CM000684.2:g.32475035C= GRCh38
NC_000022.10:g.32871022C= , CM000684.1:g.32871022C= GRCh37
NC_000022.9:g.31201022C= NCBI36
NG_016001.1:g.5316C=
NG_016001.2:g.5316C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.33C= MANE Select ENSP00000266087.7:p.Thr11=
ENST00000266087.11:c.33C= ENSP00000266087.7:p.Thr11=
ENST00000420700.5:c.33C= ENSP00000406155.1:p.Thr11=
ENST00000425028.5:c.33C= ENSP00000395823.1:p.Thr11=
ENST00000492535.1:n.21C=
NM_012179.3:c.33C= NP_036311.3:p.Thr11=
XM_011530106.1:c.-141C= XP_011528408.1:n.-141C=
XM_024452207.1:c.-158C= XP_024307975.1:n.-158C=
NM_012179.4:c.33C= MANE Select NP_036311.3:p.Thr11=