Canonical Allele Identifier: CA2496064601
Gene: FBXO11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47823166G= , CM000664.2:g.47823166G= GRCh38
NC_000002.11:g.48050305G= , CM000664.1:g.48050305G= GRCh37
NC_000002.10:g.47903809G= NCBI36
NG_008397.1:g.87510C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681999.1:n.1470C=
ENST00000682451.1:n.1439C=
ENST00000682975.1:n.1488C=
ENST00000683894.1:c.1341C= ENSP00000507789.1:p.Thr447=
ENST00000684085.1:n.1470C=
ENST00000684712.1:n.1701C=
ENST00000403359.8:c.1593C= MANE Select ENSP00000384823.4:p.Thr531=
ENST00000316377.8:c.1359C= ENSP00000323822.5:p.Thr453=
ENST00000402508.5:c.1341C= ENSP00000385398.1:p.Thr447=
ENST00000403359.7:c.1593C= ENSP00000384823.3:p.Thr531=
ENST00000492225.5:n.1441C=
ENST00000493962.6:c.967C=
NM_001190274.1:c.1593C= NP_001177203.1:p.Thr531=
NM_025133.4:c.1341C= NP_079409.3:p.Thr447=
XM_005264572.3:c.1593C= XP_005264629.1:p.Thr531=
XM_005264573.3:c.1590C= XP_005264630.1:p.Thr530=
XM_005264572.5:c.1593C= XP_005264629.1:p.Thr531=
XM_005264573.5:c.1590C= XP_005264630.1:p.Thr530=
XM_017005015.1:c.1590C= XP_016860504.1:p.Thr530=
XM_017005016.2:c.1341C= XP_016860505.1:p.Thr447=
XM_017005017.1:c.1341C= XP_016860506.1:p.Thr447=
NM_001190274.2:c.1593C= MANE Select NP_001177203.1:p.Thr531=
NM_001374325.1:c.1341C= NP_001361254.1:p.Thr447=