Canonical Allele Identifier: CA2401985163
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474967_32474968delinsTC , CM000684.2:g.32474967_32474968delinsTC GRCh38
NC_000022.10:g.32870954_32870955delinsTC , CM000684.1:g.32870954_32870955delinsTC GRCh37
NC_000022.9:g.31200954_31200955delinsTC NCBI36
NG_016001.1:g.5248_5249delinsTC
NG_016001.2:g.5248_5249delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-36_-35delinsTC MANE Select ENSP00000266087.7:n.-36_-35delinsTC
ENST00000266087.11:c.-36_-35delinsTC ENSP00000266087.7:n.-36_-35delinsTC
ENST00000420700.5:c.-36_-35delinsTC ENSP00000406155.1:n.-36_-35delinsTC
ENST00000425028.5:c.-36_-35delinsTC ENSP00000395823.1:n.-36_-35delinsTC
NM_012179.3:c.-36_-35delinsTC NP_036311.3:n.-36_-35delinsTC
XM_011530106.1:c.-209_-208delinsTC XP_011528408.1:n.-209_-208delinsTC
XM_024452207.1:c.-226_-225delinsTC XP_024307975.1:n.-226_-225delinsTC
NM_012179.4:c.-36_-35delinsTC MANE Select NP_036311.3:n.-36_-35delinsTC