Canonical Allele Identifier: CA2496074379

Gene: FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47839446C= , CM000664.2:g.47839446C=	GRCh38
NC_000002.11:g.48066585C= , CM000664.1:g.48066585C=	GRCh37
NC_000002.10:g.47920089C=	NCBI36
NG_008397.1:g.71230G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681999.1:n.292G=
ENST00000682451.1:n.264G=
ENST00000682975.1:n.310G=
ENST00000683894.1:c.163G=	ENSP00000507789.1:p.Val55=
ENST00000684085.1:n.292G=
ENST00000684712.1:n.523G=
ENST00000403359.8:c.415G= MANE Select	ENSP00000384823.4:p.Val139=
ENST00000316377.8:c.183G=	ENSP00000323822.5:p.Glu61=
ENST00000402508.5:c.163G=	ENSP00000385398.1:p.Val55=
ENST00000403359.7:c.415G=	ENSP00000384823.3:p.Val139=
ENST00000424163.2:c.163G=	ENSP00000392272.1:p.Val55=
ENST00000480038.1:n.378G=
ENST00000492225.5:n.263G=
NM_001190274.1:c.415G=	NP_001177203.1:p.Val139=
NM_025133.4:c.163G=	NP_079409.3:p.Val55=
XM_005264572.3:c.415G=	XP_005264629.1:p.Val139=
XM_005264573.3:c.415G=	XP_005264630.1:p.Val139=
XM_005264572.5:c.415G=	XP_005264629.1:p.Val139=
XM_005264573.5:c.415G=	XP_005264630.1:p.Val139=
XM_017005015.1:c.415G=	XP_016860504.1:p.Val139=
XM_017005016.2:c.163G=	XP_016860505.1:p.Val55=
XM_017005017.1:c.163G=	XP_016860506.1:p.Val55=
NM_001190274.2:c.415G= MANE Select	NP_001177203.1:p.Val139=
NM_001374325.1:c.163G=	NP_001361254.1:p.Val55=