Canonical Allele Identifier: CA415184449

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350190A>T , CM000685.2:g.154350190A>T	GRCh38
NC_000023.10:g.153578558A>T , CM000685.1:g.153578558A>T	GRCh37
NC_000023.9:g.153231752A>T	NCBI36
NG_011506.1:g.29449T>A
NG_011506.2:g.29449T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7150T>A	ENSP00000353467.4:p.Phe2384Ile
ENST00000369850.10:c.7174T>A MANE Select	ENSP00000358866.3:p.Phe2392Ile
ENST00000369856.8:c.7093T>A	ENSP00000358872.4:p.Phe2365Ile
ENST00000422373.6:c.3955T>A	ENSP00000416926.2:p.Phe1319Ile
ENST00000610817.5:c.7231T>A	ENSP00000480593.2:n.7231T>A
ENST00000673639.2:c.280-1500T>A
ENST00000676696.1:c.7453T>A	ENSP00000503392.1:n.7453T>A
ENST00000678304.1:n.2892T>A
ENST00000344736.8:c.7054T>A	ENSP00000358863.3:p.Phe2352Ile
ENST00000360319.8:c.7150T>A	ENSP00000353467.4:p.Phe2384Ile
ENST00000369850.7:c.7174T>A	ENSP00000358866.3:p.Phe2392Ile
ENST00000369856.7:c.7093T>A	ENSP00000358872.4:p.Phe2365Ile
ENST00000420627.5:c.7130T>A	ENSP00000408921.1:n.7130T>A
ENST00000422373.5:c.7150T>A	ENSP00000416926.1:p.Phe2384Ile
ENST00000462590.1:n.166T>A
ENST00000490936.5:n.4403T>A
ENST00000498411.1:n.68-1360T>A
ENST00000498491.5:n.215T>A
ENST00000610817.4:c.6178T>A	ENSP00000480593.1:p.Phe2060Ile
NM_001110556.1:c.7174T>A	NP_001104026.1:p.Phe2392Ile
NM_001456.3:c.7150T>A	NP_001447.2:p.Phe2384Ile
XM_011531127.1:c.7078T>A	XP_011529429.1:p.Phe2360Ile
XM_011531128.1:c.7054T>A	XP_011529430.1:p.Phe2352Ile
XM_011531129.1:c.7000T>A	XP_011529431.1:p.Phe2334Ile
XM_011531130.1:c.6976T>A	XP_011529432.1:p.Phe2326Ile
XM_011531131.1:c.6973T>A	XP_011529433.1:p.Phe2325Ile
NM_001110556.2:c.7174T>A MANE Select	NP_001104026.1:p.Phe2392Ile
NM_001456.4:c.7150T>A	NP_001447.2:p.Phe2384Ile