Canonical Allele Identifier: CA2401985109
Gene: FBXO7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474911G= , CM000684.2:g.32474911G= GRCh38
NC_000022.10:g.32870898G= , CM000684.1:g.32870898G= GRCh37
NC_000022.9:g.31200898G= NCBI36
NG_016001.1:g.5192G=
NG_016001.2:g.5192G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-92G= MANE Select ENSP00000266087.7:n.-92G=
ENST00000266087.11:c.-92G= ENSP00000266087.7:n.-92G=
ENST00000420700.5:c.-92G= ENSP00000406155.1:n.-92G=
ENST00000425028.5:c.-92G= ENSP00000395823.1:n.-92G=
NM_012179.3:c.-92G= NP_036311.3:n.-92G=
XM_011530106.1:c.-265G= XP_011528408.1:n.-265G=
XM_024452207.1:c.-282G= XP_024307975.1:n.-282G=
NM_012179.4:c.-92G= MANE Select NP_036311.3:n.-92G=
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