Canonical Allele Identifier: CA2466653277

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353310C= , CM000685.2:g.154353310C=	GRCh38
NC_000023.10:g.153581678C= , CM000685.1:g.153581678C=	GRCh37
NC_000023.9:g.153234872C=	NCBI36
NG_011506.1:g.26329G=
NG_011506.2:g.26329G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5984G=	ENSP00000353467.4:p.Arg1995=
ENST00000369850.10:c.6008G= MANE Select	ENSP00000358866.3:p.Arg2003=
ENST00000369856.8:c.5927G=	ENSP00000358872.4:p.Arg1976=
ENST00000422373.6:c.3161-635G=	ENSP00000416926.2:n.3161-635G=
ENST00000610817.5:c.6065G=	ENSP00000480593.2:n.6065G=
ENST00000673639.2:c.280-4620G=
ENST00000676696.1:c.6287G=	ENSP00000503392.1:n.6287G=
ENST00000678304.1:n.1187G=
ENST00000344736.8:c.5888G=	ENSP00000358863.3:p.Arg1963=
ENST00000360319.8:c.5984G=	ENSP00000353467.4:p.Arg1995=
ENST00000369850.7:c.6008G=	ENSP00000358866.3:p.Arg2003=
ENST00000369856.7:c.5927G=	ENSP00000358872.4:p.Arg1976=
ENST00000415241.1:c.193G=
ENST00000420627.5:c.5964G=	ENSP00000408921.1:n.5964G=
ENST00000422373.5:c.5984G=	ENSP00000416926.1:p.Arg1995=
ENST00000438732.2:c.682G=
ENST00000466325.1:n.147G=
ENST00000490936.5:n.1997G=
ENST00000610817.4:c.5844+83G=	ENSP00000480593.1:n.5844+83G=
NM_001110556.1:c.6008G=	NP_001104026.1:p.Arg2003=
NM_001456.3:c.5984G=	NP_001447.2:p.Arg1995=
XM_011531127.1:c.5912G=	XP_011529429.1:p.Arg1971=
XM_011531128.1:c.5888G=	XP_011529430.1:p.Arg1963=
XM_011531129.1:c.5834G=	XP_011529431.1:p.Arg1945=
XM_011531130.1:c.5810G=	XP_011529432.1:p.Arg1937=
XM_011531131.1:c.5807G=	XP_011529433.1:p.Arg1936=
NM_001110556.2:c.6008G= MANE Select	NP_001104026.1:p.Arg2003=
NM_001456.4:c.5984G=	NP_001447.2:p.Arg1995=