Canonical Allele Identifier: CA2466653289

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353346G= , CM000685.2:g.154353346G=	GRCh38
NC_000023.10:g.153581714G= , CM000685.1:g.153581714G=	GRCh37
NC_000023.9:g.153234908G=	NCBI36
NG_011506.1:g.26293C=
NG_011506.2:g.26293C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5948C=	ENSP00000353467.4:p.Ser1983=
ENST00000369850.10:c.5972C= MANE Select	ENSP00000358866.3:p.Ser1991=
ENST00000369856.8:c.5891C=	ENSP00000358872.4:p.Ser1964=
ENST00000422373.6:c.3161-671C=	ENSP00000416926.2:n.3161-671C=
ENST00000610817.5:c.6029C=	ENSP00000480593.2:n.6029C=
ENST00000673639.2:c.280-4656C=
ENST00000676696.1:c.6251C=	ENSP00000503392.1:n.6251C=
ENST00000678304.1:n.1151C=
ENST00000344736.8:c.5852C=	ENSP00000358863.3:p.Ser1951=
ENST00000360319.8:c.5948C=	ENSP00000353467.4:p.Ser1983=
ENST00000369850.7:c.5972C=	ENSP00000358866.3:p.Ser1991=
ENST00000369856.7:c.5891C=	ENSP00000358872.4:p.Ser1964=
ENST00000415241.1:c.157C=
ENST00000420627.5:c.5928C=	ENSP00000408921.1:n.5928C=
ENST00000422373.5:c.5948C=	ENSP00000416926.1:p.Ser1983=
ENST00000438732.2:c.646C=
ENST00000466325.1:n.111C=
ENST00000490936.5:n.1961C=
ENST00000610817.4:c.5844+47C=	ENSP00000480593.1:n.5844+47C=
NM_001110556.1:c.5972C=	NP_001104026.1:p.Ser1991=
NM_001456.3:c.5948C=	NP_001447.2:p.Ser1983=
XM_011531127.1:c.5876C=	XP_011529429.1:p.Ser1959=
XM_011531128.1:c.5852C=	XP_011529430.1:p.Ser1951=
XM_011531129.1:c.5798C=	XP_011529431.1:p.Ser1933=
XM_011531130.1:c.5774C=	XP_011529432.1:p.Ser1925=
XM_011531131.1:c.5771C=	XP_011529433.1:p.Ser1924=
NM_001110556.2:c.5972C= MANE Select	NP_001104026.1:p.Ser1991=
NM_001456.4:c.5948C=	NP_001447.2:p.Ser1983=