Canonical Allele Identifier: CA202928

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154349695G>A , CM000685.2:g.154349695G>A	GRCh38
NC_000023.10:g.153578063G>A , CM000685.1:g.153578063G>A	GRCh37
NC_000023.9:g.153231257G>A	NCBI36
NG_011506.1:g.29944C>T
NG_011506.2:g.29944C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7482C>T	ENSP00000353467.4:p.Gly2494=
ENST00000369850.10:c.7506C>T MANE Select	ENSP00000358866.3:p.Gly2502=
ENST00000369856.8:c.7425C>T	ENSP00000358872.4:p.Gly2475=
ENST00000422373.6:c.4287C>T	ENSP00000416926.2:p.Gly1429=
ENST00000610817.5:c.7563C>T	ENSP00000480593.2:n.7563C>T
ENST00000673639.2:c.280-1005C>T
ENST00000676696.1:c.7785C>T	ENSP00000503392.1:n.7785C>T
ENST00000678304.1:n.3224C>T
ENST00000344736.8:c.7386C>T	ENSP00000358863.3:p.Gly2462=
ENST00000360319.8:c.7482C>T	ENSP00000353467.4:p.Gly2494=
ENST00000369850.7:c.7506C>T	ENSP00000358866.3:p.Gly2502=
ENST00000369856.7:c.7425C>T	ENSP00000358872.4:p.Gly2475=
ENST00000420627.5:c.7462C>T	ENSP00000408921.1:n.7462C>T
ENST00000422373.5:c.7482C>T	ENSP00000416926.1:p.Gly2494=
ENST00000462590.1:n.661C>T
ENST00000490936.5:n.4735C>T
ENST00000498411.1:n.68-865C>T
ENST00000498491.5:n.547C>T
ENST00000610817.4:c.6510C>T	ENSP00000480593.1:p.Gly2170=
NM_001110556.1:c.7506C>T	NP_001104026.1:p.Gly2502=
NM_001456.3:c.7482C>T	NP_001447.2:p.Gly2494=
XM_011531127.1:c.7410C>T	XP_011529429.1:p.Gly2470=
XM_011531128.1:c.7386C>T	XP_011529430.1:p.Gly2462=
XM_011531129.1:c.7332C>T	XP_011529431.1:p.Gly2444=
XM_011531130.1:c.7308C>T	XP_011529432.1:p.Gly2436=
XM_011531131.1:c.7305C>T	XP_011529433.1:p.Gly2435=
NM_001110556.2:c.7506C>T MANE Select	NP_001104026.1:p.Gly2502=
NM_001456.4:c.7482C>T	NP_001447.2:p.Gly2494=