Canonical Allele Identifier: CA2469227

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58148778A>G , CM000665.2:g.58148778A>G	GRCh38
NC_000003.11:g.58134505A>G , CM000665.1:g.58134505A>G	GRCh37
NC_000003.10:g.58109545A>G	NCBI36
NG_012801.1:g.145379A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.1369A>G
ENST00000682871.1:c.5897A>G	ENSP00000507805.1:p.Lys1966Arg
ENST00000683925.1:n.2115A>G
ENST00000684439.1:n.2328A>G
ENST00000684506.1:c.*4570A>G	ENSP00000507728.1:n.*4570A>G
ENST00000684607.1:c.6038A>G	ENSP00000508224.1:p.Lys2013Arg
ENST00000295956.9:c.6017A>G MANE Select	ENSP00000295956.5:p.Lys2006Arg
ENST00000295956.8:c.6017A>G	ENSP00000295956.4:p.Lys2006Arg
ENST00000358537.7:c.5945A>G	ENSP00000351339.3:p.Lys1982Arg
ENST00000429972.6:c.5984A>G	ENSP00000415599.2:p.Lys1995Arg
ENST00000481470.5:n.2285A>G
ENST00000490882.5:c.6110A>G	ENSP00000420213.1:p.Lys2037Arg
ENST00000493452.5:c.5438A>G	ENSP00000418510.1:p.Lys1813Arg
NM_001164317.1:c.6110A>G	NP_001157789.1:p.Lys2037Arg
NM_001164318.1:c.5984A>G	NP_001157790.1:p.Lys1995Arg
NM_001164319.1:c.5945A>G	NP_001157791.1:p.Lys1982Arg
NM_001457.3:c.6017A>G	NP_001448.2:p.Lys2006Arg
XM_005264977.1:c.6077A>G	XP_005265034.1:p.Lys2026Arg
XM_005264978.1:c.6038A>G	XP_005265035.1:p.Lys2013Arg
XM_005264981.1:c.6110A>G	XP_005265038.1:p.Lys2037Arg
XR_940396.1:n.6255A>G
XM_005264978.2:c.6038A>G	XP_005265035.1:p.Lys2013Arg
XR_001740065.1:n.6255A>G
XR_940396.2:n.6255A>G
NM_001164317.2:c.6110A>G	NP_001157789.1:p.Lys2037Arg
NM_001164318.2:c.5984A>G	NP_001157790.1:p.Lys1995Arg
NM_001164319.2:c.5945A>G	NP_001157791.1:p.Lys1982Arg
NM_001457.4:c.6017A>G MANE Select	NP_001448.2:p.Lys2006Arg