Canonical Allele Identifier: CA1367520276

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58153623G= , CM000665.2:g.58153623G=	GRCh38
NC_000003.11:g.58139350G= , CM000665.1:g.58139350G=	GRCh37
NC_000003.10:g.58114390G=	NCBI36
NG_012801.1:g.150224G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.1968G=
ENST00000682503.1:n.816G=
ENST00000682871.1:c.6496G=	ENSP00000507805.1:p.Gly2166=
ENST00000683114.1:n.1287G=
ENST00000684439.1:n.2927G=
ENST00000684506.1:c.*5169G=	ENSP00000507728.1:n.*5169G=
ENST00000684607.1:c.6637G=	ENSP00000508224.1:p.Gly2213=
ENST00000295956.9:c.6616G= MANE Select	ENSP00000295956.5:p.Gly2206=
ENST00000295956.8:c.6616G=	ENSP00000295956.4:p.Gly2206=
ENST00000358537.7:c.6544G=	ENSP00000351339.3:p.Gly2182=
ENST00000429972.6:c.6583G=	ENSP00000415599.2:p.Gly2195=
ENST00000466455.1:c.386G=
ENST00000481470.5:n.2884G=
ENST00000490882.5:c.6709G=	ENSP00000420213.1:p.Gly2237=
ENST00000493452.5:c.6037G=	ENSP00000418510.1:p.Gly2013=
NM_001164317.1:c.6709G=	NP_001157789.1:p.Gly2237=
NM_001164318.1:c.6583G=	NP_001157790.1:p.Gly2195=
NM_001164319.1:c.6544G=	NP_001157791.1:p.Gly2182=
NM_001457.3:c.6616G=	NP_001448.2:p.Gly2206=
XM_005264977.1:c.6676G=	XP_005265034.1:p.Gly2226=
XM_005264978.1:c.6637G=	XP_005265035.1:p.Gly2213=
XM_005264978.2:c.6637G=	XP_005265035.1:p.Gly2213=
XR_001740065.1:n.6924G=
NM_001164317.2:c.6709G=	NP_001157789.1:p.Gly2237=
NM_001164318.2:c.6583G=	NP_001157790.1:p.Gly2195=
NM_001164319.2:c.6544G=	NP_001157791.1:p.Gly2182=
NM_001457.4:c.6616G= MANE Select	NP_001448.2:p.Gly2206=