Canonical Allele Identifier: CA288877

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154349767C>T , CM000685.2:g.154349767C>T	GRCh38
NC_000023.10:g.153578135C>T , CM000685.1:g.153578135C>T	GRCh37
NC_000023.9:g.153231329C>T	NCBI36
NG_011506.1:g.29872G>A
NG_011506.2:g.29872G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7410G>A	ENSP00000353467.4:p.Glu2470=
ENST00000369850.10:c.7434G>A MANE Select	ENSP00000358866.3:p.Glu2478=
ENST00000369856.8:c.7353G>A	ENSP00000358872.4:p.Glu2451=
ENST00000422373.6:c.4215G>A	ENSP00000416926.2:p.Glu1405=
ENST00000610817.5:c.7491G>A	ENSP00000480593.2:n.7491G>A
ENST00000673639.2:c.280-1077G>A
ENST00000676696.1:c.7713G>A	ENSP00000503392.1:n.7713G>A
ENST00000678304.1:n.3152G>A
ENST00000344736.8:c.7314G>A	ENSP00000358863.3:p.Glu2438=
ENST00000360319.8:c.7410G>A	ENSP00000353467.4:p.Glu2470=
ENST00000369850.7:c.7434G>A	ENSP00000358866.3:p.Glu2478=
ENST00000369856.7:c.7353G>A	ENSP00000358872.4:p.Glu2451=
ENST00000420627.5:c.7390G>A	ENSP00000408921.1:n.7390G>A
ENST00000422373.5:c.7410G>A	ENSP00000416926.1:p.Glu2470=
ENST00000462590.1:n.589G>A
ENST00000490936.5:n.4663G>A
ENST00000498411.1:n.68-937G>A
ENST00000498491.5:n.475G>A
ENST00000610817.4:c.6438G>A	ENSP00000480593.1:p.Glu2146=
NM_001110556.1:c.7434G>A	NP_001104026.1:p.Glu2478=
NM_001456.3:c.7410G>A	NP_001447.2:p.Glu2470=
XM_011531127.1:c.7338G>A	XP_011529429.1:p.Glu2446=
XM_011531128.1:c.7314G>A	XP_011529430.1:p.Glu2438=
XM_011531129.1:c.7260G>A	XP_011529431.1:p.Glu2420=
XM_011531130.1:c.7236G>A	XP_011529432.1:p.Glu2412=
XM_011531131.1:c.7233G>A	XP_011529433.1:p.Glu2411=
NM_001110556.2:c.7434G>A MANE Select	NP_001104026.1:p.Glu2478=
NM_001456.4:c.7410G>A	NP_001447.2:p.Glu2470=