Canonical Allele Identifier: CA2656311169
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474774dup , CM000684.2:g.32474774dup GRCh38
NC_000022.10:g.32870761dup , CM000684.1:g.32870761dup GRCh37
NC_000022.9:g.31200761dup NCBI36
NG_016001.1:g.5055dup
NG_016001.2:g.5055dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-229dup ENSP00000266087.7:n.-229dup
ENST00000420700.5:c.-229dup ENSP00000406155.1:n.-229dup
NM_012179.3:c.-229dup NP_036311.3:n.-229dup
XM_011530106.1:c.-402dup XP_011528408.1:n.-402dup
XM_024452207.1:c.-419dup XP_024307975.1:n.-419dup