Canonical Allele Identifier: CA2656311288
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474840_32474856del , CM000684.2:g.32474840_32474856del GRCh38
NC_000022.10:g.32870827_32870843del , CM000684.1:g.32870827_32870843del GRCh37
NC_000022.9:g.31200827_31200843del NCBI36
NG_016001.1:g.5121_5137del
NG_016001.2:g.5121_5137del

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-163_-147del MANE Select ENSP00000266087.7:n.-163_-147del
ENST00000266087.11:c.-163_-147del ENSP00000266087.7:n.-163_-147del
ENST00000420700.5:c.-163_-147del ENSP00000406155.1:n.-163_-147del
ENST00000425028.5:c.-163_-147del ENSP00000395823.1:n.-163_-147del
NM_012179.3:c.-163_-147del NP_036311.3:n.-163_-147del
XM_011530106.1:c.-336_-320del XP_011528408.1:n.-336_-320del
XM_024452207.1:c.-353_-337del XP_024307975.1:n.-353_-337del
NM_012179.4:c.-163_-147del MANE Select NP_036311.3:n.-163_-147del