Canonical Allele Identifier: CA2496064557
Gene: FBXO11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47823081T= , CM000664.2:g.47823081T= GRCh38
NC_000002.11:g.48050220T= , CM000664.1:g.48050220T= GRCh37
NC_000002.10:g.47903724T= NCBI36
NG_008397.1:g.87595A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681999.1:n.1493+62A=
ENST00000682451.1:n.1462+62A=
ENST00000682975.1:n.1511+62A=
ENST00000683894.1:c.1364+62A= ENSP00000507789.1:n.1364+62A=
ENST00000684085.1:n.1493+62A=
ENST00000684712.1:n.1724+62A=
ENST00000403359.8:c.1616+62A= MANE Select ENSP00000384823.4:n.1616+62A=
ENST00000316377.8:c.1382+62A= ENSP00000323822.5:n.1382+62A=
ENST00000402508.5:c.1364+62A= ENSP00000385398.1:n.1364+62A=
ENST00000403359.7:c.1616+62A= ENSP00000384823.3:n.1616+62A=
ENST00000492225.5:n.1464+62A=
ENST00000493962.6:c.990+62A=
NM_001190274.1:c.1616+62A= NP_001177203.1:n.1616+62A=
NM_025133.4:c.1364+62A= NP_079409.3:n.1364+62A=
XM_005264572.3:c.1616+62A= XP_005264629.1:n.1616+62A=
XM_005264573.3:c.1613+62A= XP_005264630.1:n.1613+62A=
XM_005264572.5:c.1616+62A= XP_005264629.1:n.1616+62A=
XM_005264573.5:c.1613+62A= XP_005264630.1:n.1613+62A=
XM_017005015.1:c.1613+62A= XP_016860504.1:n.1613+62A=
XM_017005016.2:c.1364+62A= XP_016860505.1:n.1364+62A=
XM_017005017.1:c.1364+62A= XP_016860506.1:n.1364+62A=
NM_001190274.2:c.1616+62A= MANE Select NP_001177203.1:n.1616+62A=
NM_001374325.1:c.1364+62A= NP_001361254.1:n.1364+62A=