Canonical Allele Identifier: CA2466653287

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353341G= , CM000685.2:g.154353341G=	GRCh38
NC_000023.10:g.153581709G= , CM000685.1:g.153581709G=	GRCh37
NC_000023.9:g.153234903G=	NCBI36
NG_011506.1:g.26298C=
NG_011506.2:g.26298C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5953C=	ENSP00000353467.4:p.Arg1985=
ENST00000369850.10:c.5977C= MANE Select	ENSP00000358866.3:p.Arg1993=
ENST00000369856.8:c.5896C=	ENSP00000358872.4:p.Arg1966=
ENST00000422373.6:c.3161-666C=	ENSP00000416926.2:n.3161-666C=
ENST00000610817.5:c.6034C=	ENSP00000480593.2:n.6034C=
ENST00000673639.2:c.280-4651C=
ENST00000676696.1:c.6256C=	ENSP00000503392.1:n.6256C=
ENST00000678304.1:n.1156C=
ENST00000344736.8:c.5857C=	ENSP00000358863.3:p.Arg1953=
ENST00000360319.8:c.5953C=	ENSP00000353467.4:p.Arg1985=
ENST00000369850.7:c.5977C=	ENSP00000358866.3:p.Arg1993=
ENST00000369856.7:c.5896C=	ENSP00000358872.4:p.Arg1966=
ENST00000415241.1:c.162C=
ENST00000420627.5:c.5933C=	ENSP00000408921.1:n.5933C=
ENST00000422373.5:c.5953C=	ENSP00000416926.1:p.Arg1985=
ENST00000438732.2:c.651C=
ENST00000466325.1:n.116C=
ENST00000490936.5:n.1966C=
ENST00000610817.4:c.5844+52C=	ENSP00000480593.1:n.5844+52C=
NM_001110556.1:c.5977C=	NP_001104026.1:p.Arg1993=
NM_001456.3:c.5953C=	NP_001447.2:p.Arg1985=
XM_011531127.1:c.5881C=	XP_011529429.1:p.Arg1961=
XM_011531128.1:c.5857C=	XP_011529430.1:p.Arg1953=
XM_011531129.1:c.5803C=	XP_011529431.1:p.Arg1935=
XM_011531130.1:c.5779C=	XP_011529432.1:p.Arg1927=
XM_011531131.1:c.5776C=	XP_011529433.1:p.Arg1926=
NM_001110556.2:c.5977C= MANE Select	NP_001104026.1:p.Arg1993=
NM_001456.4:c.5953C=	NP_001447.2:p.Arg1985=