Canonical Allele Identifier: CA2466653224

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353173C= , CM000685.2:g.154353173C=	GRCh38
NC_000023.10:g.153581541C= , CM000685.1:g.153581541C=	GRCh37
NC_000023.9:g.153234735C=	NCBI36
NG_011506.1:g.26466G=
NG_011506.2:g.26466G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6030G=	ENSP00000353467.4:p.Glu2010=
ENST00000369850.10:c.6054G= MANE Select	ENSP00000358866.3:p.Glu2018=
ENST00000369856.8:c.5973G=	ENSP00000358872.4:p.Glu1991=
ENST00000422373.6:c.3161-498G=	ENSP00000416926.2:n.3161-498G=
ENST00000610817.5:c.6111G=	ENSP00000480593.2:n.6111G=
ENST00000673639.2:c.280-4483G=
ENST00000676696.1:c.6333G=	ENSP00000503392.1:n.6333G=
ENST00000678304.1:n.1233G=
ENST00000344736.8:c.5934G=	ENSP00000358863.3:p.Glu1978=
ENST00000360319.8:c.6030G=	ENSP00000353467.4:p.Glu2010=
ENST00000369850.7:c.6054G=	ENSP00000358866.3:p.Glu2018=
ENST00000369856.7:c.5973G=	ENSP00000358872.4:p.Glu1991=
ENST00000415241.1:c.256G=
ENST00000420627.5:c.6010G=	ENSP00000408921.1:n.6010G=
ENST00000422373.5:c.6030G=	ENSP00000416926.1:p.Glu2010=
ENST00000466325.1:n.193G=
ENST00000490936.5:n.2043G=
ENST00000610817.4:c.5844+220G=	ENSP00000480593.1:n.5844+220G=
NM_001110556.1:c.6054G=	NP_001104026.1:p.Glu2018=
NM_001456.3:c.6030G=	NP_001447.2:p.Glu2010=
XM_011531127.1:c.5958G=	XP_011529429.1:p.Glu1986=
XM_011531128.1:c.5934G=	XP_011529430.1:p.Glu1978=
XM_011531129.1:c.5880G=	XP_011529431.1:p.Glu1960=
XM_011531130.1:c.5856G=	XP_011529432.1:p.Glu1952=
XM_011531131.1:c.5853G=	XP_011529433.1:p.Glu1951=
NM_001110556.2:c.6054G= MANE Select	NP_001104026.1:p.Glu2018=
NM_001456.4:c.6030G=	NP_001447.2:p.Glu2010=