Canonical Allele Identifier: CA288874

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350140G>A , CM000685.2:g.154350140G>A	GRCh38
NC_000023.10:g.153578508G>A , CM000685.1:g.153578508G>A	GRCh37
NC_000023.9:g.153231702G>A	NCBI36
NG_011506.1:g.29499C>T
NG_011506.2:g.29499C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7200C>T	ENSP00000353467.4:p.Gly2400=
ENST00000369850.10:c.7224C>T MANE Select	ENSP00000358866.3:p.Gly2408=
ENST00000369856.8:c.7143C>T	ENSP00000358872.4:p.Gly2381=
ENST00000422373.6:c.4005C>T	ENSP00000416926.2:p.Gly1335=
ENST00000610817.5:c.7281C>T	ENSP00000480593.2:n.7281C>T
ENST00000673639.2:c.280-1450C>T
ENST00000676696.1:c.7503C>T	ENSP00000503392.1:n.7503C>T
ENST00000678304.1:n.2942C>T
ENST00000344736.8:c.7104C>T	ENSP00000358863.3:p.Gly2368=
ENST00000360319.8:c.7200C>T	ENSP00000353467.4:p.Gly2400=
ENST00000369850.7:c.7224C>T	ENSP00000358866.3:p.Gly2408=
ENST00000369856.7:c.7143C>T	ENSP00000358872.4:p.Gly2381=
ENST00000420627.5:c.7180C>T	ENSP00000408921.1:n.7180C>T
ENST00000422373.5:c.7200C>T	ENSP00000416926.1:p.Gly2400=
ENST00000462590.1:n.216C>T
ENST00000490936.5:n.4453C>T
ENST00000498411.1:n.68-1310C>T
ENST00000498491.5:n.265C>T
ENST00000610817.4:c.6228C>T	ENSP00000480593.1:p.Gly2076=
NM_001110556.1:c.7224C>T	NP_001104026.1:p.Gly2408=
NM_001456.3:c.7200C>T	NP_001447.2:p.Gly2400=
XM_011531127.1:c.7128C>T	XP_011529429.1:p.Gly2376=
XM_011531128.1:c.7104C>T	XP_011529430.1:p.Gly2368=
XM_011531129.1:c.7050C>T	XP_011529431.1:p.Gly2350=
XM_011531130.1:c.7026C>T	XP_011529432.1:p.Gly2342=
XM_011531131.1:c.7023C>T	XP_011529433.1:p.Gly2341=
NM_001110556.2:c.7224C>T MANE Select	NP_001104026.1:p.Gly2408=
NM_001456.4:c.7200C>T	NP_001447.2:p.Gly2400=