Canonical Allele Identifier: CA2469661

Gene: FLNB FLNB-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58168601G>A , CM000665.2:g.58168601G>A	GRCh38
NC_000003.11:g.58154328G>A , CM000665.1:g.58154328G>A	GRCh37
NC_000003.10:g.58129368G>A	NCBI36
NG_012801.1:g.165202G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419752.4:n.4029G>A (FLNB)
ENST00000682297.1:n.2712G>A (FLNB)
ENST00000682503.1:n.1560G>A (FLNB)
ENST00000682871.1:c.7240G>A (FLNB)	ENSP00000507805.1:p.Val2414Ile
ENST00000683114.1:n.2031G>A (FLNB)
ENST00000684439.1:n.3671G>A (FLNB)
ENST00000684506.1:c.*5913G>A (FLNB)	ENSP00000507728.1:n.*5913G>A
ENST00000684607.1:c.*452G>A (FLNB)	ENSP00000508224.1:n.*452G>A
ENST00000295956.9:c.7360G>A (FLNB) MANE Select	ENSP00000295956.5:p.Val2454Ile
ENST00000295956.8:c.7360G>A (FLNB)	ENSP00000295956.4:p.Val2454Ile
ENST00000358537.7:c.7288G>A (FLNB)	ENSP00000351339.3:p.Val2430Ile
ENST00000419752.3:c.40G>A (FLNB)	ENSP00000414532.3:p.Val14Ile
ENST00000429972.6:c.7327G>A (FLNB)	ENSP00000415599.2:p.Val2443Ile
ENST00000481470.5:n.3628G>A (FLNB)
ENST00000484981.1:n.267G>A (FLNB)
ENST00000490882.5:c.7453G>A (FLNB)	ENSP00000420213.1:p.Val2485Ile
ENST00000493452.5:c.6781G>A (FLNB)	ENSP00000418510.1:p.Val2261Ile
NM_001164317.1:c.7453G>A (FLNB)	NP_001157789.1:p.Val2485Ile
NM_001164318.1:c.7327G>A (FLNB)	NP_001157790.1:p.Val2443Ile
NM_001164319.1:c.7288G>A (FLNB)	NP_001157791.1:p.Val2430Ile
NM_001457.3:c.7360G>A (FLNB)	NP_001448.2:p.Val2454Ile
XM_005264977.1:c.7420G>A (FLNB)	XP_005265034.1:p.Val2474Ile
XM_005264978.1:c.7381G>A (FLNB)	XP_005265035.1:p.Val2461Ile
XR_940875.1:n.139+1896C>T (FLNB-AS1)
NR_135534.1:n.139+1896C>T (FLNB-AS1)
XM_005264978.2:c.7381G>A (FLNB)	XP_005265035.1:p.Val2461Ile
XR_001740065.1:n.7668G>A (FLNB)
NM_001164317.2:c.7453G>A (FLNB)	NP_001157789.1:p.Val2485Ile
NM_001164318.2:c.7327G>A (FLNB)	NP_001157790.1:p.Val2443Ile
NM_001164319.2:c.7288G>A (FLNB)	NP_001157791.1:p.Val2430Ile
NM_001457.4:c.7360G>A (FLNB) MANE Select	NP_001448.2:p.Val2454Ile