Canonical Allele Identifier: CA2469416

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58153522G>A , CM000665.2:g.58153522G>A	GRCh38
NC_000003.11:g.58139249G>A , CM000665.1:g.58139249G>A	GRCh37
NC_000003.10:g.58114289G>A	NCBI36
NG_012801.1:g.150123G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.1867G>A
ENST00000682503.1:n.715G>A
ENST00000682871.1:c.6395G>A	ENSP00000507805.1:p.Arg2132His
ENST00000683114.1:n.1186G>A
ENST00000684439.1:n.2826G>A
ENST00000684506.1:c.*5068G>A	ENSP00000507728.1:n.*5068G>A
ENST00000684607.1:c.6536G>A	ENSP00000508224.1:p.Arg2179His
ENST00000295956.9:c.6515G>A MANE Select	ENSP00000295956.5:p.Arg2172His
ENST00000295956.8:c.6515G>A	ENSP00000295956.4:p.Arg2172His
ENST00000358537.7:c.6443G>A	ENSP00000351339.3:p.Arg2148His
ENST00000429972.6:c.6482G>A	ENSP00000415599.2:p.Arg2161His
ENST00000466455.1:c.285G>A
ENST00000481470.5:n.2783G>A
ENST00000490882.5:c.6608G>A	ENSP00000420213.1:p.Arg2203His
ENST00000493452.5:c.5936G>A	ENSP00000418510.1:p.Arg1979His
NM_001164317.1:c.6608G>A	NP_001157789.1:p.Arg2203His
NM_001164318.1:c.6482G>A	NP_001157790.1:p.Arg2161His
NM_001164319.1:c.6443G>A	NP_001157791.1:p.Arg2148His
NM_001457.3:c.6515G>A	NP_001448.2:p.Arg2172His
XM_005264977.1:c.6575G>A	XP_005265034.1:p.Arg2192His
XM_005264978.1:c.6536G>A	XP_005265035.1:p.Arg2179His
XM_005264978.2:c.6536G>A	XP_005265035.1:p.Arg2179His
XR_001740065.1:n.6823G>A
NM_001164317.2:c.6608G>A	NP_001157789.1:p.Arg2203His
NM_001164318.2:c.6482G>A	NP_001157790.1:p.Arg2161His
NM_001164319.2:c.6443G>A	NP_001157791.1:p.Arg2148His
NM_001457.4:c.6515G>A MANE Select	NP_001448.2:p.Arg2172His