Canonical Allele Identifier: CA303002

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154349432G>A , CM000685.2:g.154349432G>A	GRCh38
NC_000023.10:g.153577800G>A , CM000685.1:g.153577800G>A	GRCh37
NC_000023.9:g.153230994G>A	NCBI36
NG_011506.1:g.30207C>T
NG_011506.2:g.30207C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7662C>T	ENSP00000353467.4:p.Ala2554=
ENST00000369850.10:c.7686C>T MANE Select	ENSP00000358866.3:p.Ala2562=
ENST00000369856.8:c.7605C>T	ENSP00000358872.4:p.Ala2535=
ENST00000422373.6:c.4467C>T	ENSP00000416926.2:p.Ala1489=
ENST00000610817.5:c.7743C>T	ENSP00000480593.2:n.7743C>T
ENST00000673639.2:c.280-742C>T
ENST00000676696.1:c.7965C>T	ENSP00000503392.1:n.7965C>T
ENST00000678304.1:n.3404C>T
ENST00000344736.8:c.7566C>T	ENSP00000358863.3:p.Ala2522=
ENST00000360319.8:c.7662C>T	ENSP00000353467.4:p.Ala2554=
ENST00000369850.7:c.7686C>T	ENSP00000358866.3:p.Ala2562=
ENST00000369856.7:c.7605C>T	ENSP00000358872.4:p.Ala2535=
ENST00000420627.5:c.7642C>T	ENSP00000408921.1:n.7642C>T
ENST00000422373.5:c.7662C>T	ENSP00000416926.1:p.Ala2554=
ENST00000462590.1:n.841C>T
ENST00000490936.5:n.4915C>T
ENST00000498411.1:n.68-602C>T
ENST00000498491.5:n.727C>T
ENST00000610817.4:c.6690C>T	ENSP00000480593.1:p.Ala2230=
NM_001110556.1:c.7686C>T	NP_001104026.1:p.Ala2562=
NM_001456.3:c.7662C>T	NP_001447.2:p.Ala2554=
XM_011531127.1:c.7590C>T	XP_011529429.1:p.Ala2530=
XM_011531128.1:c.7566C>T	XP_011529430.1:p.Ala2522=
XM_011531129.1:c.7512C>T	XP_011529431.1:p.Ala2504=
XM_011531130.1:c.7488C>T	XP_011529432.1:p.Ala2496=
XM_011531131.1:c.7485C>T	XP_011529433.1:p.Ala2495=
NM_001110556.2:c.7686C>T MANE Select	NP_001104026.1:p.Ala2562=
NM_001456.4:c.7662C>T	NP_001447.2:p.Ala2554=