Canonical Allele Identifier: CA426008141

Gene: FBXO11

Linked Data

• MyVariant Identifiers: chr2:g.48050290T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47823151T>G , CM000664.2:g.47823151T>G	GRCh38
NC_000002.11:g.48050290T>G , CM000664.1:g.48050290T>G	GRCh37
NC_000002.10:g.47903794T>G	NCBI36
NG_008397.1:g.87525A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000681999.1:n.1485A>C
ENST00000682451.1:n.1454A>C
ENST00000682975.1:n.1503A>C
ENST00000683894.1:c.1356A>C	ENSP00000507789.1:p.Pro452=
ENST00000684085.1:n.1485A>C
ENST00000684712.1:n.1716A>C
ENST00000403359.8:c.1608A>C MANE Select	ENSP00000384823.4:p.Pro536=
ENST00000316377.8:c.1374A>C	ENSP00000323822.5:p.Pro458=
ENST00000402508.5:c.1356A>C	ENSP00000385398.1:p.Pro452=
ENST00000403359.7:c.1608A>C	ENSP00000384823.3:p.Pro536=
ENST00000492225.5:n.1456A>C
ENST00000493962.6:c.982A>C
NM_001190274.1:c.1608A>C	NP_001177203.1:p.Pro536=
NM_025133.4:c.1356A>C	NP_079409.3:p.Pro452=
XM_005264572.3:c.1608A>C	XP_005264629.1:p.Pro536=
XM_005264573.3:c.1605A>C	XP_005264630.1:p.Pro535=
XM_005264572.5:c.1608A>C	XP_005264629.1:p.Pro536=
XM_005264573.5:c.1605A>C	XP_005264630.1:p.Pro535=
XM_017005015.1:c.1605A>C	XP_016860504.1:p.Pro535=
XM_017005016.2:c.1356A>C	XP_016860505.1:p.Pro452=
XM_017005017.1:c.1356A>C	XP_016860506.1:p.Pro452=
NM_001190274.2:c.1608A>C MANE Select	NP_001177203.1:p.Pro536=
NM_001374325.1:c.1356A>C	NP_001361254.1:p.Pro452=