Canonical Allele Identifier: CA10559868

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154349559C>T , CM000685.2:g.154349559C>T	GRCh38
NC_000023.10:g.153577927C>T , CM000685.1:g.153577927C>T	GRCh37
NC_000023.9:g.153231121C>T	NCBI36
NG_011506.1:g.30080G>A
NG_011506.2:g.30080G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001110556.2:c.7559G>A MANE Select	NP_001104026.1:p.Arg2520His
ENST00000369850.10:c.7559G>A MANE Select	ENSP00000358866.3:p.Arg2520His
NM_001110556.1:c.7559G>A	NP_001104026.1:p.Arg2520His
NM_001456.3:c.7535G>A	NP_001447.2:p.Arg2512His
NM_001456.4:c.7535G>A	NP_001447.2:p.Arg2512His
ENST00000344736.8:c.7439G>A	ENSP00000358863.3:p.Arg2480His
ENST00000360319.8:c.7535G>A	ENSP00000353467.4:p.Arg2512His
ENST00000360319.9:c.7535G>A	ENSP00000353467.4:p.Arg2512His
ENST00000369850.7:c.7559G>A	ENSP00000358866.3:p.Arg2520His
ENST00000369856.7:c.7478G>A	ENSP00000358872.4:p.Arg2493His
ENST00000369856.8:c.7478G>A	ENSP00000358872.4:p.Arg2493His
ENST00000420627.5:c.7515G>A	ENSP00000408921.1:n.7515G>A
ENST00000422373.5:c.7535G>A	ENSP00000416926.1:p.Arg2512His
ENST00000422373.6:c.4340G>A	ENSP00000416926.2:p.Arg1447His
ENST00000462590.1:n.714G>A
ENST00000490936.5:n.4788G>A
ENST00000498411.1:n.68-729G>A
ENST00000498491.5:n.600G>A
ENST00000610817.4:c.6563G>A	ENSP00000480593.1:p.Arg2188His
ENST00000610817.5:c.7616G>A	ENSP00000480593.2:n.7616G>A
ENST00000673639.2:c.280-869G>A
ENST00000676696.1:c.7838G>A	ENSP00000503392.1:n.7838G>A
ENST00000678304.1:n.3277G>A
XM_011531127.1:c.7463G>A	XP_011529429.1:p.Arg2488His
XM_011531128.1:c.7439G>A	XP_011529430.1:p.Arg2480His
XM_011531129.1:c.7385G>A	XP_011529431.1:p.Arg2462His
XM_011531130.1:c.7361G>A	XP_011529432.1:p.Arg2454His
XM_011531131.1:c.7358G>A	XP_011529433.1:p.Arg2453His