Canonical Allele Identifier: CA657983108
Gene: FBXO7 HGNC NCBI

Linked Data

COSMIC: COSN24315737
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474969_32474970insT , CM000684.2:g.32474969_32474970insT GRCh38
NC_000022.10:g.32870956_32870957insT , CM000684.1:g.32870956_32870957insT GRCh37
NC_000022.9:g.31200956_31200957insT NCBI36
NG_016001.1:g.5250_5251insT
NG_016001.2:g.5250_5251insT

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-34_-33insT MANE Select ENSP00000266087.7:n.-34_-33insT
ENST00000266087.11:c.-34_-33insT ENSP00000266087.7:n.-34_-33insT
ENST00000420700.5:c.-34_-33insT ENSP00000406155.1:n.-34_-33insT
ENST00000425028.5:c.-34_-33insT ENSP00000395823.1:n.-34_-33insT
NM_012179.3:c.-34_-33insT NP_036311.3:n.-34_-33insT
XM_011530106.1:c.-207_-206insT XP_011528408.1:n.-207_-206insT
XM_024452207.1:c.-224_-223insT XP_024307975.1:n.-224_-223insT
NM_012179.4:c.-34_-33insT MANE Select NP_036311.3:n.-34_-33insT
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