Canonical Allele Identifier: CA2401985344
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475248G= , CM000684.2:g.32475248G= GRCh38
NC_000022.10:g.32871235G= , CM000684.1:g.32871235G= GRCh37
NC_000022.9:g.31201235G= NCBI36
NG_016001.1:g.5529G=
NG_016001.2:g.5529G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.122+124G= MANE Select ENSP00000266087.7:n.122+124G=
ENST00000266087.11:c.122+124G= ENSP00000266087.7:n.122+124G=
ENST00000420700.5:c.122+124G= ENSP00000406155.1:n.122+124G=
ENST00000425028.5:c.122+124G= ENSP00000395823.1:n.122+124G=
ENST00000452138.3:c.-114G= ENSP00000388547.2:n.-114G=
ENST00000492535.1:n.110+124G=
NM_001033024.1:c.-114G= NP_001028196.1:n.-114G=
NM_001257990.1:c.-371G= NP_001244919.1:n.-371G=
NM_012179.3:c.122+124G= NP_036311.3:n.122+124G=
XM_011530106.1:c.-52+124G= XP_011528408.1:n.-52+124G=
XM_024452207.1:c.-69+124G= XP_024307975.1:n.-69+124G=
NM_012179.4:c.122+124G= MANE Select NP_036311.3:n.122+124G=