Canonical Allele Identifier: CA2656311417
Gene: FBXO7 HGNC NCBI

Linked Data

gnomAD v4: 22-32474945-CGCCGCCGTCCCCGTCGCCGCTTCCGGGTCCAGGCCCCTCGGGCCGCCT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474955_32475002del , CM000684.2:g.32474955_32475002del GRCh38
NC_000022.10:g.32870942_32870989del , CM000684.1:g.32870942_32870989del GRCh37
NC_000022.9:g.31200942_31200989del NCBI36
NG_016001.1:g.5236_5283del
NG_016001.2:g.5236_5283del

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-48_-1del MANE Select ENSP00000266087.7:n.-48_-1del
ENST00000266087.11:c.-48_-1del ENSP00000266087.7:n.-48_-1del
ENST00000420700.5:c.-48_-1del ENSP00000406155.1:n.-48_-1del
ENST00000425028.5:c.-48_-1del ENSP00000395823.1:n.-48_-1del
NM_012179.3:c.-48_-1del NP_036311.3:n.-48_-1del
XM_011530106.1:c.-221_-174del XP_011528408.1:n.-221_-174del
XM_024452207.1:c.-238_-191del XP_024307975.1:n.-238_-191del
NM_012179.4:c.-48_-1del MANE Select NP_036311.3:n.-48_-1del
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