Canonical Allele Identifier: CA411329899
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475056G>T , CM000684.2:g.32475056G>T GRCh38
NC_000022.10:g.32871043G>T , CM000684.1:g.32871043G>T GRCh37
NC_000022.9:g.31201043G>T NCBI36
NG_016001.1:g.5337G>T
NG_016001.2:g.5337G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.54G>T MANE Select ENSP00000266087.7:p.Glu18Asp
ENST00000266087.11:c.54G>T ENSP00000266087.7:p.Glu18Asp
ENST00000420700.5:c.54G>T ENSP00000406155.1:p.Glu18Asp
ENST00000425028.5:c.54G>T ENSP00000395823.1:p.Glu18Asp
ENST00000492535.1:n.42G>T
NM_012179.3:c.54G>T NP_036311.3:p.Glu18Asp
XM_011530106.1:c.-120G>T XP_011528408.1:n.-120G>T
XM_024452207.1:c.-137G>T XP_024307975.1:n.-137G>T
NM_012179.4:c.54G>T MANE Select NP_036311.3:p.Glu18Asp