Canonical Allele Identifier: CA2469601

Gene: FLNB FLNB-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58163231G>A , CM000665.2:g.58163231G>A	GRCh38
NC_000003.11:g.58148958G>A , CM000665.1:g.58148958G>A	GRCh37
NC_000003.10:g.58123998G>A	NCBI36
NG_012801.1:g.159832G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.2451G>A (FLNB)
ENST00000682503.1:n.1299G>A (FLNB)
ENST00000682871.1:c.6979G>A (FLNB)	ENSP00000507805.1:p.Val2327Ile
ENST00000683114.1:n.1770G>A (FLNB)
ENST00000684439.1:n.3410G>A (FLNB)
ENST00000684506.1:c.*5652G>A (FLNB)	ENSP00000507728.1:n.*5652G>A
ENST00000684607.1:c.*191G>A (FLNB)	ENSP00000508224.1:n.*191G>A
ENST00000295956.9:c.7099G>A (FLNB) MANE Select	ENSP00000295956.5:p.Val2367Ile
ENST00000295956.8:c.7099G>A (FLNB)	ENSP00000295956.4:p.Val2367Ile
ENST00000358537.7:c.7027G>A (FLNB)	ENSP00000351339.3:p.Val2343Ile
ENST00000429972.6:c.7066G>A (FLNB)	ENSP00000415599.2:p.Val2356Ile
ENST00000475487.1:n.260G>A (FLNB)
ENST00000481470.5:n.3367G>A (FLNB)
ENST00000490882.5:c.7192G>A (FLNB)	ENSP00000420213.1:p.Val2398Ile
ENST00000493452.5:c.6520G>A (FLNB)	ENSP00000418510.1:p.Val2174Ile
NM_001164317.1:c.7192G>A (FLNB)	NP_001157789.1:p.Val2398Ile
NM_001164318.1:c.7066G>A (FLNB)	NP_001157790.1:p.Val2356Ile
NM_001164319.1:c.7027G>A (FLNB)	NP_001157791.1:p.Val2343Ile
NM_001457.3:c.7099G>A (FLNB)	NP_001448.2:p.Val2367Ile
XM_005264977.1:c.7159G>A (FLNB)	XP_005265034.1:p.Val2387Ile
XM_005264978.1:c.7120G>A (FLNB)	XP_005265035.1:p.Val2374Ile
XR_940875.1:n.3024C>T (FLNB-AS1)
NR_135534.1:n.3024C>T (FLNB-AS1)
XM_005264978.2:c.7120G>A (FLNB)	XP_005265035.1:p.Val2374Ile
XR_001740065.1:n.7407G>A (FLNB)
NM_001164317.2:c.7192G>A (FLNB)	NP_001157789.1:p.Val2398Ile
NM_001164318.2:c.7066G>A (FLNB)	NP_001157790.1:p.Val2356Ile
NM_001164319.2:c.7027G>A (FLNB)	NP_001157791.1:p.Val2343Ile
NM_001457.4:c.7099G>A (FLNB) MANE Select	NP_001448.2:p.Val2367Ile