Canonical Allele Identifier: CA2656311449
Gene: FBXO7 HGNC NCBI

Linked Data

gnomAD v4: 22-32474984-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474987del , CM000684.2:g.32474987del GRCh38
NC_000022.10:g.32870974del , CM000684.1:g.32870974del GRCh37
NC_000022.9:g.31200974del NCBI36
NG_016001.1:g.5268del
NG_016001.2:g.5268del

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-16del MANE Select ENSP00000266087.7:n.-16del
ENST00000266087.11:c.-16del ENSP00000266087.7:n.-16del
ENST00000420700.5:c.-16del ENSP00000406155.1:n.-16del
ENST00000425028.5:c.-16del ENSP00000395823.1:n.-16del
NM_012179.3:c.-16del NP_036311.3:n.-16del
XM_011530106.1:c.-189del XP_011528408.1:n.-189del
XM_024452207.1:c.-206del XP_024307975.1:n.-206del
NM_012179.4:c.-16del MANE Select NP_036311.3:n.-16del
Search 100 bp 5'
Search 100 bp 3'