Canonical Allele Identifier: CA346813326

Gene: FBXO11

Linked Data

• MyVariant Identifiers: chr2:g.48066568T>G (hg19) ; chr2:g.47839429T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47839429T>G , CM000664.2:g.47839429T>G	GRCh38
NC_000002.11:g.48066568T>G , CM000664.1:g.48066568T>G	GRCh37
NC_000002.10:g.47920072T>G	NCBI36
NG_008397.1:g.71247A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681999.1:n.309A>C
ENST00000682451.1:n.281A>C
ENST00000682975.1:n.327A>C
ENST00000683894.1:c.180A>C	ENSP00000507789.1:p.Gln60His
ENST00000684085.1:n.309A>C
ENST00000684712.1:n.540A>C
ENST00000403359.8:c.432A>C MANE Select	ENSP00000384823.4:p.Gln144His
ENST00000316377.8:c.198A>C	ENSP00000323822.5:p.Gln66His
ENST00000402508.5:c.180A>C	ENSP00000385398.1:p.Gln60His
ENST00000403359.7:c.432A>C	ENSP00000384823.3:p.Gln144His
ENST00000424163.2:c.180A>C	ENSP00000392272.1:p.Gln60His
ENST00000480038.1:n.395A>C
ENST00000492225.5:n.280A>C
NM_001190274.1:c.432A>C	NP_001177203.1:p.Gln144His
NM_025133.4:c.180A>C	NP_079409.3:p.Gln60His
XM_005264572.3:c.432A>C	XP_005264629.1:p.Gln144His
XM_005264573.3:c.432A>C	XP_005264630.1:p.Gln144His
XM_005264572.5:c.432A>C	XP_005264629.1:p.Gln144His
XM_005264573.5:c.432A>C	XP_005264630.1:p.Gln144His
XM_017005015.1:c.432A>C	XP_016860504.1:p.Gln144His
XM_017005016.2:c.180A>C	XP_016860505.1:p.Gln60His
XM_017005017.1:c.180A>C	XP_016860506.1:p.Gln60His
NM_001190274.2:c.432A>C MANE Select	NP_001177203.1:p.Gln144His
NM_001374325.1:c.180A>C	NP_001361254.1:p.Gln60His