Canonical Allele Identifier: CA411329875
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.43G>T MANE Select ENSP00000266087.7:p.Glu15Ter
ENST00000266087.11:c.43G>T ENSP00000266087.7:p.Glu15Ter
ENST00000420700.5:c.43G>T ENSP00000406155.1:p.Glu15Ter
ENST00000425028.5:c.43G>T ENSP00000395823.1:p.Glu15Ter
ENST00000492535.1:n.31G>T
NM_012179.3:c.43G>T NP_036311.3:p.Glu15Ter
XM_011530106.1:c.-131G>T XP_011528408.1:n.-131G>T
XM_024452207.1:c.-148G>T XP_024307975.1:n.-148G>T
NM_012179.4:c.43G>T MANE Select NP_036311.3:p.Glu15Ter