Canonical Allele Identifier: CA1025186463
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs2057417928
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475137_32475142del , CM000684.2:g.32475137_32475142del GRCh38
NC_000022.10:g.32871124_32871129del , CM000684.1:g.32871124_32871129del GRCh37
NC_000022.9:g.31201124_31201129del NCBI36
NG_016001.1:g.5418_5423del
NG_016001.2:g.5418_5423del

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.122+13_122+18del MANE Select ENSP00000266087.7:n.122+13_122+18del
ENST00000266087.11:c.122+13_122+18del ENSP00000266087.7:n.122+13_122+18del
ENST00000420700.5:c.122+13_122+18del ENSP00000406155.1:n.122+13_122+18del
ENST00000425028.5:c.122+13_122+18del ENSP00000395823.1:n.122+13_122+18del
ENST00000492535.1:n.110+13_110+18del
NM_012179.3:c.122+13_122+18del NP_036311.3:n.122+13_122+18del
XM_011530106.1:c.-52+13_-52+18del XP_011528408.1:n.-52+13_-52+18del
XM_024452207.1:c.-69+13_-69+18del XP_024307975.1:n.-69+13_-69+18del
NM_012179.4:c.122+13_122+18del MANE Select NP_036311.3:n.122+13_122+18del
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