Canonical Allele Identifier: CA2401989545
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32484543_32484544delinsTA , CM000684.2:g.32484543_32484544delinsTA GRCh38
NC_000022.10:g.32880530_32880531delinsTA , CM000684.1:g.32880530_32880531delinsTA GRCh37
NC_000022.9:g.31210530_31210531delinsTA NCBI36
NG_016001.1:g.14824_14825delinsTA
NG_016001.2:g.14824_14825delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.645+419_645+420delinsTA MANE Select ENSP00000266087.7:n.645+419_645+420delinsTA
ENST00000266087.11:c.645+419_645+420delinsTA ENSP00000266087.7:n.645+419_645+420delinsTA
ENST00000397426.5:c.303+419_303+420delinsTA ENSP00000380571.1:n.303+419_303+420delinsTA
ENST00000420700.5:c.*224+419_*224+420delinsTA ENSP00000406155.1:n.*224+419_*224+420delinsTA
ENST00000425028.5:c.*343+419_*343+420delinsTA ENSP00000395823.1:n.*343+419_*343+420delinsTA
ENST00000452138.3:c.408+419_408+420delinsTA ENSP00000388547.2:n.408+419_408+420delinsTA
ENST00000492535.1:n.481+419_481+420delinsTA
NM_001033024.1:c.408+419_408+420delinsTA NP_001028196.1:n.408+419_408+420delinsTA
NM_001257990.1:c.303+419_303+420delinsTA NP_001244919.1:n.303+419_303+420delinsTA
NM_012179.3:c.645+419_645+420delinsTA NP_036311.3:n.645+419_645+420delinsTA
XM_011530106.1:c.177+419_177+420delinsTA XP_011528408.1:n.177+419_177+420delinsTA
XM_024452207.1:c.303+419_303+420delinsTA XP_024307975.1:n.303+419_303+420delinsTA
NM_012179.4:c.645+419_645+420delinsTA MANE Select NP_036311.3:n.645+419_645+420delinsTA
NM_001033024.2:c.408+419_408+420delinsTA NP_001028196.1:n.408+419_408+420delinsTA
NM_001257990.2:c.303+419_303+420delinsTA NP_001244919.1:n.303+419_303+420delinsTA