Canonical Allele Identifier: CA2466653061

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352776C= , CM000685.2:g.154352776C=	GRCh38
NC_000023.10:g.153581144C= , CM000685.1:g.153581144C=	GRCh37
NC_000023.9:g.153234338C=	NCBI36
NG_011506.1:g.26863G=
NG_011506.2:g.26863G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6351G=	ENSP00000353467.4:p.Val2117=
ENST00000369850.10:c.6375G= MANE Select	ENSP00000358866.3:p.Val2125=
ENST00000369856.8:c.6294G=	ENSP00000358872.4:p.Val2098=
ENST00000422373.6:c.3161-101G=	ENSP00000416926.2:n.3161-101G=
ENST00000610817.5:c.6432G=	ENSP00000480593.2:n.6432G=
ENST00000673639.2:c.280-4086G=
ENST00000676696.1:c.6654G=	ENSP00000503392.1:n.6654G=
ENST00000678304.1:n.1554G=
ENST00000344736.8:c.6255G=	ENSP00000358863.3:p.Val2085=
ENST00000360319.8:c.6351G=	ENSP00000353467.4:p.Val2117=
ENST00000369850.7:c.6375G=	ENSP00000358866.3:p.Val2125=
ENST00000369856.7:c.6294G=	ENSP00000358872.4:p.Val2098=
ENST00000415241.1:c.577G=
ENST00000420627.5:c.6331G=	ENSP00000408921.1:n.6331G=
ENST00000422373.5:c.6351G=	ENSP00000416926.1:p.Val2117=
ENST00000444578.1:c.318G=	ENSP00000397824.1:p.Val106=
ENST00000466325.1:n.590G=
ENST00000474358.5:n.8G=
ENST00000490936.5:n.2364G=
ENST00000498411.1:n.67+41G=
ENST00000610817.4:c.5844+617G=	ENSP00000480593.1:n.5844+617G=
NM_001110556.1:c.6375G=	NP_001104026.1:p.Val2125=
NM_001456.3:c.6351G=	NP_001447.2:p.Val2117=
XM_011531127.1:c.6279G=	XP_011529429.1:p.Val2093=
XM_011531128.1:c.6255G=	XP_011529430.1:p.Val2085=
XM_011531129.1:c.6201G=	XP_011529431.1:p.Val2067=
XM_011531130.1:c.6177G=	XP_011529432.1:p.Val2059=
XM_011531131.1:c.6174G=	XP_011529433.1:p.Val2058=
NM_001110556.2:c.6375G= MANE Select	NP_001104026.1:p.Val2125=
NM_001456.4:c.6351G=	NP_001447.2:p.Val2117=