Canonical Allele Identifier: CA411329984
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475096C>T , CM000684.2:g.32475096C>T GRCh38
NC_000022.10:g.32871083C>T , CM000684.1:g.32871083C>T GRCh37
NC_000022.9:g.31201083C>T NCBI36
NG_016001.1:g.5377C>T
NG_016001.2:g.5377C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.94C>T MANE Select ENSP00000266087.7:p.Gln32Ter
ENST00000266087.11:c.94C>T ENSP00000266087.7:p.Gln32Ter
ENST00000420700.5:c.94C>T ENSP00000406155.1:p.Gln32Ter
ENST00000425028.5:c.94C>T ENSP00000395823.1:p.Gln32Ter
ENST00000492535.1:n.82C>T
NM_012179.3:c.94C>T NP_036311.3:p.Gln32Ter
XM_011530106.1:c.-80C>T XP_011528408.1:n.-80C>T
XM_024452207.1:c.-97C>T XP_024307975.1:n.-97C>T
NM_012179.4:c.94C>T MANE Select NP_036311.3:p.Gln32Ter