Canonical Allele Identifier: CA2656311280
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474833del , CM000684.2:g.32474833del GRCh38
NC_000022.10:g.32870820del , CM000684.1:g.32870820del GRCh37
NC_000022.9:g.31200820del NCBI36
NG_016001.1:g.5114del
NG_016001.2:g.5114del

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-170del MANE Select ENSP00000266087.7:n.-170del
ENST00000266087.11:c.-170del ENSP00000266087.7:n.-170del
ENST00000420700.5:c.-170del ENSP00000406155.1:n.-170del
ENST00000425028.5:c.-170del ENSP00000395823.1:n.-170del
NM_012179.3:c.-170del NP_036311.3:n.-170del
XM_011530106.1:c.-343del XP_011528408.1:n.-343del
XM_024452207.1:c.-360del XP_024307975.1:n.-360del
NM_012179.4:c.-170del MANE Select NP_036311.3:n.-170del