Canonical Allele Identifier: CA1367516857

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58146043G= , CM000665.2:g.58146043G=	GRCh38
NC_000003.11:g.58131770G= , CM000665.1:g.58131770G=	GRCh37
NC_000003.10:g.58106810G=	NCBI36
NG_012801.1:g.142644G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.900G=
ENST00000682871.1:c.5428G=	ENSP00000507805.1:p.Gly1810=
ENST00000683925.1:n.1646G=
ENST00000684439.1:n.1859G=
ENST00000684506.1:c.*4101G=	ENSP00000507728.1:n.*4101G=
ENST00000684607.1:c.5569G=	ENSP00000508224.1:p.Gly1857=
ENST00000295956.9:c.5548G= MANE Select	ENSP00000295956.5:p.Gly1850=
ENST00000295956.8:c.5548G=	ENSP00000295956.4:p.Gly1850=
ENST00000358537.7:c.5476G=	ENSP00000351339.3:p.Gly1826=
ENST00000429972.6:c.5515G=	ENSP00000415599.2:p.Gly1839=
ENST00000481470.5:n.1816G=
ENST00000490882.5:c.5641G=	ENSP00000420213.1:p.Gly1881=
ENST00000493452.5:c.4969G=	ENSP00000418510.1:p.Gly1657=
NM_001164317.1:c.5641G=	NP_001157789.1:p.Gly1881=
NM_001164318.1:c.5515G=	NP_001157790.1:p.Gly1839=
NM_001164319.1:c.5476G=	NP_001157791.1:p.Gly1826=
NM_001457.3:c.5548G=	NP_001448.2:p.Gly1850=
XM_005264977.1:c.5608G=	XP_005265034.1:p.Gly1870=
XM_005264978.1:c.5569G=	XP_005265035.1:p.Gly1857=
XM_005264981.1:c.5641G=	XP_005265038.1:p.Gly1881=
XR_940396.1:n.5786G=
XM_005264978.2:c.5569G=	XP_005265035.1:p.Gly1857=
XR_001740065.1:n.5786G=
XR_940396.2:n.5786G=
NM_001164317.2:c.5641G=	NP_001157789.1:p.Gly1881=
NM_001164318.2:c.5515G=	NP_001157790.1:p.Gly1839=
NM_001164319.2:c.5476G=	NP_001157791.1:p.Gly1826=
NM_001457.4:c.5548G= MANE Select	NP_001448.2:p.Gly1850=