Canonical Allele Identifier: CA2401985256
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475128C= , CM000684.2:g.32475128C= GRCh38
NC_000022.10:g.32871115C= , CM000684.1:g.32871115C= GRCh37
NC_000022.9:g.31201115C= NCBI36
NG_016001.1:g.5409C=
NG_016001.2:g.5409C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.122+4C= MANE Select ENSP00000266087.7:n.122+4C=
ENST00000266087.11:c.122+4C= ENSP00000266087.7:n.122+4C=
ENST00000420700.5:c.122+4C= ENSP00000406155.1:n.122+4C=
ENST00000425028.5:c.122+4C= ENSP00000395823.1:n.122+4C=
ENST00000492535.1:n.110+4C=
NM_012179.3:c.122+4C= NP_036311.3:n.122+4C=
XM_011530106.1:c.-52+4C= XP_011528408.1:n.-52+4C=
XM_024452207.1:c.-69+4C= XP_024307975.1:n.-69+4C=
NM_012179.4:c.122+4C= MANE Select NP_036311.3:n.122+4C=