Canonical Allele Identifier: CA2401985220
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475064C= , CM000684.2:g.32475064C= GRCh38
NC_000022.10:g.32871051C= , CM000684.1:g.32871051C= GRCh37
NC_000022.9:g.31201051C= NCBI36
NG_016001.1:g.5345C=
NG_016001.2:g.5345C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.62C= MANE Select ENSP00000266087.7:p.Pro21=
ENST00000266087.11:c.62C= ENSP00000266087.7:p.Pro21=
ENST00000420700.5:c.62C= ENSP00000406155.1:p.Pro21=
ENST00000425028.5:c.62C= ENSP00000395823.1:p.Pro21=
ENST00000492535.1:n.50C=
NM_012179.3:c.62C= NP_036311.3:p.Pro21=
XM_011530106.1:c.-112C= XP_011528408.1:n.-112C=
XM_024452207.1:c.-129C= XP_024307975.1:n.-129C=
NM_012179.4:c.62C= MANE Select NP_036311.3:p.Pro21=