Canonical Allele Identifier: CA411329921
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475066A>C , CM000684.2:g.32475066A>C GRCh38
NC_000022.10:g.32871053A>C , CM000684.1:g.32871053A>C GRCh37
NC_000022.9:g.31201053A>C NCBI36
NG_016001.1:g.5347A>C
NG_016001.2:g.5347A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.64A>C MANE Select ENSP00000266087.7:p.Thr22Pro
ENST00000266087.11:c.64A>C ENSP00000266087.7:p.Thr22Pro
ENST00000420700.5:c.64A>C ENSP00000406155.1:p.Thr22Pro
ENST00000425028.5:c.64A>C ENSP00000395823.1:p.Thr22Pro
ENST00000492535.1:n.52A>C
NM_012179.3:c.64A>C NP_036311.3:p.Thr22Pro
XM_011530106.1:c.-110A>C XP_011528408.1:n.-110A>C
XM_024452207.1:c.-127A>C XP_024307975.1:n.-127A>C
NM_012179.4:c.64A>C MANE Select NP_036311.3:p.Thr22Pro