Canonical Allele Identifier: CA346764658
Gene: FBXO11 HGNC NCBI

Linked Data

gnomAD v4: 2-47823153-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47823153G>T , CM000664.2:g.47823153G>T GRCh38
NC_000002.11:g.48050292G>T , CM000664.1:g.48050292G>T GRCh37
NC_000002.10:g.47903796G>T NCBI36
NG_008397.1:g.87523C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000681999.1:n.1483C>A
ENST00000682451.1:n.1452C>A
ENST00000682975.1:n.1501C>A
ENST00000683894.1:c.1354C>A ENSP00000507789.1:p.Pro452Thr
ENST00000684085.1:n.1483C>A
ENST00000684712.1:n.1714C>A
ENST00000403359.8:c.1606C>A MANE Select ENSP00000384823.4:p.Pro536Thr
ENST00000316377.8:c.1372C>A ENSP00000323822.5:p.Pro458Thr
ENST00000402508.5:c.1354C>A ENSP00000385398.1:p.Pro452Thr
ENST00000403359.7:c.1606C>A ENSP00000384823.3:p.Pro536Thr
ENST00000492225.5:n.1454C>A
ENST00000493962.6:c.980C>A
NM_001190274.1:c.1606C>A NP_001177203.1:p.Pro536Thr
NM_025133.4:c.1354C>A NP_079409.3:p.Pro452Thr
XM_005264572.3:c.1606C>A XP_005264629.1:p.Pro536Thr
XM_005264573.3:c.1603C>A XP_005264630.1:p.Pro535Thr
XM_005264572.5:c.1606C>A XP_005264629.1:p.Pro536Thr
XM_005264573.5:c.1603C>A XP_005264630.1:p.Pro535Thr
XM_017005015.1:c.1603C>A XP_016860504.1:p.Pro535Thr
XM_017005016.2:c.1354C>A XP_016860505.1:p.Pro452Thr
XM_017005017.1:c.1354C>A XP_016860506.1:p.Pro452Thr
NM_001190274.2:c.1606C>A MANE Select NP_001177203.1:p.Pro536Thr
NM_001374325.1:c.1354C>A NP_001361254.1:p.Pro452Thr