Canonical Allele Identifier: CA411329874
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475045G>C , CM000684.2:g.32475045G>C GRCh38
NC_000022.10:g.32871032G>C , CM000684.1:g.32871032G>C GRCh37
NC_000022.9:g.31201032G>C NCBI36
NG_016001.1:g.5326G>C
NG_016001.2:g.5326G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.43G>C MANE Select ENSP00000266087.7:p.Glu15Gln
ENST00000266087.11:c.43G>C ENSP00000266087.7:p.Glu15Gln
ENST00000420700.5:c.43G>C ENSP00000406155.1:p.Glu15Gln
ENST00000425028.5:c.43G>C ENSP00000395823.1:p.Glu15Gln
ENST00000492535.1:n.31G>C
NM_012179.3:c.43G>C NP_036311.3:p.Glu15Gln
XM_011530106.1:c.-131G>C XP_011528408.1:n.-131G>C
XM_024452207.1:c.-148G>C XP_024307975.1:n.-148G>C
NM_012179.4:c.43G>C MANE Select NP_036311.3:p.Glu15Gln