Canonical Allele Identifier: CA2401985059
Gene: FBXO7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474812C= , CM000684.2:g.32474812C= GRCh38
NC_000022.10:g.32870799C= , CM000684.1:g.32870799C= GRCh37
NC_000022.9:g.31200799C= NCBI36
NG_016001.1:g.5093C=
NG_016001.2:g.5093C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-191C= MANE Select ENSP00000266087.7:n.-191C=
ENST00000266087.11:c.-191C= ENSP00000266087.7:n.-191C=
ENST00000420700.5:c.-191C= ENSP00000406155.1:n.-191C=
ENST00000425028.5:c.-191C= ENSP00000395823.1:n.-191C=
NM_012179.3:c.-191C= NP_036311.3:n.-191C=
XM_011530106.1:c.-364C= XP_011528408.1:n.-364C=
XM_024452207.1:c.-381C= XP_024307975.1:n.-381C=
NM_012179.4:c.-191C= MANE Select NP_036311.3:n.-191C=
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