Canonical Allele Identifier: CA2401985139
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474948_32474949delinsCG , CM000684.2:g.32474948_32474949delinsCG GRCh38
NC_000022.10:g.32870935_32870936delinsCG , CM000684.1:g.32870935_32870936delinsCG GRCh37
NC_000022.9:g.31200935_31200936delinsCG NCBI36
NG_016001.1:g.5229_5230delinsCG
NG_016001.2:g.5229_5230delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-55_-54delinsCG MANE Select ENSP00000266087.7:n.-55_-54delinsCG
ENST00000266087.11:c.-55_-54delinsCG ENSP00000266087.7:n.-55_-54delinsCG
ENST00000420700.5:c.-55_-54delinsCG ENSP00000406155.1:n.-55_-54delinsCG
ENST00000425028.5:c.-55_-54delinsCG ENSP00000395823.1:n.-55_-54delinsCG
NM_012179.3:c.-55_-54delinsCG NP_036311.3:n.-55_-54delinsCG
XM_011530106.1:c.-228_-227delinsCG XP_011528408.1:n.-228_-227delinsCG
XM_024452207.1:c.-245_-244delinsCG XP_024307975.1:n.-245_-244delinsCG
NM_012179.4:c.-55_-54delinsCG MANE Select NP_036311.3:n.-55_-54delinsCG