Canonical Allele Identifier: CA346764661

Gene: FBXO11

Linked Data

• MyVariant Identifiers: chr2:g.48050294T>G (hg19) ; chr2:g.47823155T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47823155T>G , CM000664.2:g.47823155T>G	GRCh38
NC_000002.11:g.48050294T>G , CM000664.1:g.48050294T>G	GRCh37
NC_000002.10:g.47903798T>G	NCBI36
NG_008397.1:g.87521A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000681999.1:n.1481A>C
ENST00000682451.1:n.1450A>C
ENST00000682975.1:n.1499A>C
ENST00000683894.1:c.1352A>C	ENSP00000507789.1:p.Asp451Ala
ENST00000684085.1:n.1481A>C
ENST00000684712.1:n.1712A>C
ENST00000403359.8:c.1604A>C MANE Select	ENSP00000384823.4:p.Asp535Ala
ENST00000316377.8:c.1370A>C	ENSP00000323822.5:p.Asp457Ala
ENST00000402508.5:c.1352A>C	ENSP00000385398.1:p.Asp451Ala
ENST00000403359.7:c.1604A>C	ENSP00000384823.3:p.Asp535Ala
ENST00000492225.5:n.1452A>C
ENST00000493962.6:c.978A>C
NM_001190274.1:c.1604A>C	NP_001177203.1:p.Asp535Ala
NM_025133.4:c.1352A>C	NP_079409.3:p.Asp451Ala
XM_005264572.3:c.1604A>C	XP_005264629.1:p.Asp535Ala
XM_005264573.3:c.1601A>C	XP_005264630.1:p.Asp534Ala
XM_005264572.5:c.1604A>C	XP_005264629.1:p.Asp535Ala
XM_005264573.5:c.1601A>C	XP_005264630.1:p.Asp534Ala
XM_017005015.1:c.1601A>C	XP_016860504.1:p.Asp534Ala
XM_017005016.2:c.1352A>C	XP_016860505.1:p.Asp451Ala
XM_017005017.1:c.1352A>C	XP_016860506.1:p.Asp451Ala
NM_001190274.2:c.1604A>C MANE Select	NP_001177203.1:p.Asp535Ala
NM_001374325.1:c.1352A>C	NP_001361254.1:p.Asp451Ala