Canonical Allele Identifier: CA2466653189

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353076G= , CM000685.2:g.154353076G=	GRCh38
NC_000023.10:g.153581444G= , CM000685.1:g.153581444G=	GRCh37
NC_000023.9:g.153234638G=	NCBI36
NG_011506.1:g.26563C=
NG_011506.2:g.26563C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6127C=	ENSP00000353467.4:p.Arg2043=
ENST00000369850.10:c.6151C= MANE Select	ENSP00000358866.3:p.Arg2051=
ENST00000369856.8:c.6070C=	ENSP00000358872.4:p.Arg2024=
ENST00000422373.6:c.3161-401C=	ENSP00000416926.2:n.3161-401C=
ENST00000610817.5:c.6208C=	ENSP00000480593.2:n.6208C=
ENST00000673639.2:c.280-4386C=
ENST00000676696.1:c.6430C=	ENSP00000503392.1:n.6430C=
ENST00000678304.1:n.1330C=
ENST00000344736.8:c.6031C=	ENSP00000358863.3:p.Arg2011=
ENST00000360319.8:c.6127C=	ENSP00000353467.4:p.Arg2043=
ENST00000369850.7:c.6151C=	ENSP00000358866.3:p.Arg2051=
ENST00000369856.7:c.6070C=	ENSP00000358872.4:p.Arg2024=
ENST00000415241.1:c.353C=
ENST00000420627.5:c.6107C=	ENSP00000408921.1:n.6107C=
ENST00000422373.5:c.6127C=	ENSP00000416926.1:p.Arg2043=
ENST00000444578.1:c.94C=	ENSP00000397824.1:p.Arg32=
ENST00000466325.1:n.290C=
ENST00000490936.5:n.2140C=
ENST00000610817.4:c.5844+317C=	ENSP00000480593.1:n.5844+317C=
NM_001110556.1:c.6151C=	NP_001104026.1:p.Arg2051=
NM_001456.3:c.6127C=	NP_001447.2:p.Arg2043=
XM_011531127.1:c.6055C=	XP_011529429.1:p.Arg2019=
XM_011531128.1:c.6031C=	XP_011529430.1:p.Arg2011=
XM_011531129.1:c.5977C=	XP_011529431.1:p.Arg1993=
XM_011531130.1:c.5953C=	XP_011529432.1:p.Arg1985=
XM_011531131.1:c.5950C=	XP_011529433.1:p.Arg1984=
NM_001110556.2:c.6151C= MANE Select	NP_001104026.1:p.Arg2051=
NM_001456.4:c.6127C=	NP_001447.2:p.Arg2043=