Canonical Allele Identifier: CA2401985203
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475031_32475036delinsGGACCT , CM000684.2:g.32475031_32475036delinsGGACCT GRCh38
NC_000022.10:g.32871018_32871023delinsGGACCT , CM000684.1:g.32871018_32871023delinsGGACCT GRCh37
NC_000022.9:g.31201018_31201023delinsGGACCT NCBI36
NG_016001.1:g.5312_5317delinsGGACCT
NG_016001.2:g.5312_5317delinsGGACCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.29_34delinsGGACCT MANE Select ENSP00000266087.7:p.Arg10=
ENST00000266087.11:c.29_34delinsGGACCT ENSP00000266087.7:p.Arg10=
ENST00000420700.5:c.29_34delinsGGACCT ENSP00000406155.1:p.Arg10=
ENST00000425028.5:c.29_34delinsGGACCT ENSP00000395823.1:p.Arg10=
ENST00000492535.1:n.17_22delinsGGACCT
NM_012179.3:c.29_34delinsGGACCT NP_036311.3:p.Arg10=
XM_011530106.1:c.-145_-140delinsGGACCT XP_011528408.1:n.-145_-140delinsGGACCT
XM_024452207.1:c.-162_-157delinsGGACCT XP_024307975.1:n.-162_-157delinsGGACCT
NM_012179.4:c.29_34delinsGGACCT MANE Select NP_036311.3:p.Arg10=