Canonical Allele Identifier: CA1367524252

Gene: FLNB FLNB-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58163161T= , CM000665.2:g.58163161T=	GRCh38
NC_000003.11:g.58148888T= , CM000665.1:g.58148888T=	GRCh37
NC_000003.10:g.58123928T=	NCBI36
NG_012801.1:g.159762T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.2381T= (FLNB)
ENST00000682503.1:n.1229T= (FLNB)
ENST00000682871.1:c.6909T= (FLNB)	ENSP00000507805.1:p.Tyr2303=
ENST00000683114.1:n.1700T= (FLNB)
ENST00000684439.1:n.3340T= (FLNB)
ENST00000684506.1:c.*5582T= (FLNB)	ENSP00000507728.1:n.*5582T=
ENST00000684607.1:c.*121T= (FLNB)	ENSP00000508224.1:n.*121T=
ENST00000295956.9:c.7029T= (FLNB) MANE Select	ENSP00000295956.5:p.Tyr2343=
ENST00000295956.8:c.7029T= (FLNB)	ENSP00000295956.4:p.Tyr2343=
ENST00000358537.7:c.6957T= (FLNB)	ENSP00000351339.3:p.Tyr2319=
ENST00000429972.6:c.6996T= (FLNB)	ENSP00000415599.2:p.Tyr2332=
ENST00000475487.1:n.190T= (FLNB)
ENST00000481470.5:n.3297T= (FLNB)
ENST00000490882.5:c.7122T= (FLNB)	ENSP00000420213.1:p.Tyr2374=
ENST00000493452.5:c.6450T= (FLNB)	ENSP00000418510.1:p.Tyr2150=
NM_001164317.1:c.7122T= (FLNB)	NP_001157789.1:p.Tyr2374=
NM_001164318.1:c.6996T= (FLNB)	NP_001157790.1:p.Tyr2332=
NM_001164319.1:c.6957T= (FLNB)	NP_001157791.1:p.Tyr2319=
NM_001457.3:c.7029T= (FLNB)	NP_001448.2:p.Tyr2343=
XM_005264977.1:c.7089T= (FLNB)	XP_005265034.1:p.Tyr2363=
XM_005264978.1:c.7050T= (FLNB)	XP_005265035.1:p.Tyr2350=
XR_940875.1:n.3094A= (FLNB-AS1)
NR_135534.1:n.3094A= (FLNB-AS1)
XM_005264978.2:c.7050T= (FLNB)	XP_005265035.1:p.Tyr2350=
XR_001740065.1:n.7337T= (FLNB)
NM_001164317.2:c.7122T= (FLNB)	NP_001157789.1:p.Tyr2374=
NM_001164318.2:c.6996T= (FLNB)	NP_001157790.1:p.Tyr2332=
NM_001164319.2:c.6957T= (FLNB)	NP_001157791.1:p.Tyr2319=
NM_001457.4:c.7029T= (FLNB) MANE Select	NP_001448.2:p.Tyr2343=