Canonical Allele Identifier: CA2466653084

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352831C= , CM000685.2:g.154352831C=	GRCh38
NC_000023.10:g.153581199C= , CM000685.1:g.153581199C=	GRCh37
NC_000023.9:g.153234393C=	NCBI36
NG_011506.1:g.26808G=
NG_011506.2:g.26808G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6296G=	ENSP00000353467.4:p.Cys2099=
ENST00000369850.10:c.6320G= MANE Select	ENSP00000358866.3:p.Cys2107=
ENST00000369856.8:c.6239G=	ENSP00000358872.4:p.Cys2080=
ENST00000422373.6:c.3161-156G=	ENSP00000416926.2:n.3161-156G=
ENST00000610817.5:c.6377G=	ENSP00000480593.2:n.6377G=
ENST00000673639.2:c.280-4141G=
ENST00000676696.1:c.6599G=	ENSP00000503392.1:n.6599G=
ENST00000678304.1:n.1499G=
ENST00000344736.8:c.6200G=	ENSP00000358863.3:p.Cys2067=
ENST00000360319.8:c.6296G=	ENSP00000353467.4:p.Cys2099=
ENST00000369850.7:c.6320G=	ENSP00000358866.3:p.Cys2107=
ENST00000369856.7:c.6239G=	ENSP00000358872.4:p.Cys2080=
ENST00000415241.1:c.522G=
ENST00000420627.5:c.6276G=	ENSP00000408921.1:n.6276G=
ENST00000422373.5:c.6296G=	ENSP00000416926.1:p.Cys2099=
ENST00000444578.1:c.263G=	ENSP00000397824.1:p.Cys88=
ENST00000466325.1:n.535G=
ENST00000490936.5:n.2309G=
ENST00000498411.1:n.53G=
ENST00000610817.4:c.5844+562G=	ENSP00000480593.1:n.5844+562G=
NM_001110556.1:c.6320G=	NP_001104026.1:p.Cys2107=
NM_001456.3:c.6296G=	NP_001447.2:p.Cys2099=
XM_011531127.1:c.6224G=	XP_011529429.1:p.Cys2075=
XM_011531128.1:c.6200G=	XP_011529430.1:p.Cys2067=
XM_011531129.1:c.6146G=	XP_011529431.1:p.Cys2049=
XM_011531130.1:c.6122G=	XP_011529432.1:p.Cys2041=
XM_011531131.1:c.6119G=	XP_011529433.1:p.Cys2040=
NM_001110556.2:c.6320G= MANE Select	NP_001104026.1:p.Cys2107=
NM_001456.4:c.6296G=	NP_001447.2:p.Cys2099=