Canonical Allele Identifier: CA2658970366

Gene: FBXO11

Linked Data

• gnomAD v4: 2-47822997-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47822997A>G , CM000664.2:g.47822997A>G	GRCh38
NC_000002.11:g.48050136A>G , CM000664.1:g.48050136A>G	GRCh37
NC_000002.10:g.47903640A>G	NCBI36
NG_008397.1:g.87679T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000681999.1:n.1493+146T>C
ENST00000682451.1:n.1462+146T>C
ENST00000682975.1:n.1511+146T>C
ENST00000683894.1:c.1364+146T>C	ENSP00000507789.1:n.1364+146T>C
ENST00000684085.1:n.1493+146T>C
ENST00000684712.1:n.1724+146T>C
ENST00000403359.8:c.1616+146T>C MANE Select	ENSP00000384823.4:n.1616+146T>C
ENST00000316377.8:c.1382+146T>C	ENSP00000323822.5:n.1382+146T>C
ENST00000402508.5:c.1364+146T>C	ENSP00000385398.1:n.1364+146T>C
ENST00000403359.7:c.1616+146T>C	ENSP00000384823.3:n.1616+146T>C
ENST00000492225.5:n.1464+146T>C
ENST00000493962.6:c.990+146T>C
NM_001190274.1:c.1616+146T>C	NP_001177203.1:n.1616+146T>C
NM_025133.4:c.1364+146T>C	NP_079409.3:n.1364+146T>C
XM_005264572.3:c.1616+146T>C	XP_005264629.1:n.1616+146T>C
XM_005264573.3:c.1613+146T>C	XP_005264630.1:n.1613+146T>C
XM_005264572.5:c.1616+146T>C	XP_005264629.1:n.1616+146T>C
XM_005264573.5:c.1613+146T>C	XP_005264630.1:n.1613+146T>C
XM_017005015.1:c.1613+146T>C	XP_016860504.1:n.1613+146T>C
XM_017005016.2:c.1364+146T>C	XP_016860505.1:n.1364+146T>C
XM_017005017.1:c.1364+146T>C	XP_016860506.1:n.1364+146T>C
NM_001190274.2:c.1616+146T>C MANE Select	NP_001177203.1:n.1616+146T>C
NM_001374325.1:c.1364+146T>C	NP_001361254.1:n.1364+146T>C