Canonical Allele Identifier: CA16616644

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154348991C>T , CM000685.2:g.154348991C>T	GRCh38
NC_000023.10:g.153577359C>T , CM000685.1:g.153577359C>T	GRCh37
NC_000023.9:g.153230553C>T	NCBI36
NG_011506.1:g.30648G>A
NG_011506.2:g.30648G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7778G>A	ENSP00000353467.4:p.Cys2593Tyr
ENST00000369850.10:c.7802G>A MANE Select	ENSP00000358866.3:p.Cys2601Tyr
ENST00000369856.8:c.7721G>A	ENSP00000358872.4:p.Cys2574Tyr
ENST00000422373.6:c.4583G>A	ENSP00000416926.2:p.Cys1528Tyr
ENST00000610817.5:c.7859G>A	ENSP00000480593.2:n.7859G>A
ENST00000673639.2:c.280-301G>A
ENST00000676696.1:c.8081G>A	ENSP00000503392.1:n.8081G>A
ENST00000678304.1:n.3520G>A
ENST00000344736.8:c.7682G>A	ENSP00000358863.3:p.Cys2561Tyr
ENST00000360319.8:c.7778G>A	ENSP00000353467.4:p.Cys2593Tyr
ENST00000369850.7:c.7802G>A	ENSP00000358866.3:p.Cys2601Tyr
ENST00000369856.7:c.7721G>A	ENSP00000358872.4:p.Cys2574Tyr
ENST00000420627.5:c.7758G>A	ENSP00000408921.1:n.7758G>A
ENST00000422373.5:c.7778G>A	ENSP00000416926.1:p.Cys2593Tyr
ENST00000462590.1:n.957G>A
ENST00000490936.5:n.5031G>A
ENST00000498411.1:n.68-161G>A
ENST00000498491.5:n.843G>A
ENST00000610817.4:c.6806G>A	ENSP00000480593.1:p.Cys2269Tyr
NM_001110556.1:c.7802G>A	NP_001104026.1:p.Cys2601Tyr
NM_001456.3:c.7778G>A	NP_001447.2:p.Cys2593Tyr
XM_011531127.1:c.7706G>A	XP_011529429.1:p.Cys2569Tyr
XM_011531128.1:c.7682G>A	XP_011529430.1:p.Cys2561Tyr
XM_011531129.1:c.7628G>A	XP_011529431.1:p.Cys2543Tyr
XM_011531130.1:c.7604G>A	XP_011529432.1:p.Cys2535Tyr
XM_011531131.1:c.7601G>A	XP_011529433.1:p.Cys2534Tyr
NM_001110556.2:c.7802G>A MANE Select	NP_001104026.1:p.Cys2601Tyr
NM_001456.4:c.7778G>A	NP_001447.2:p.Cys2593Tyr