Canonical Allele Identifier: CA2466653191

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353082G= , CM000685.2:g.154353082G=	GRCh38
NC_000023.10:g.153581450G= , CM000685.1:g.153581450G=	GRCh37
NC_000023.9:g.153234644G=	NCBI36
NG_011506.1:g.26557C=
NG_011506.2:g.26557C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6121C=	ENSP00000353467.4:p.Arg2041=
ENST00000369850.10:c.6145C= MANE Select	ENSP00000358866.3:p.Arg2049=
ENST00000369856.8:c.6064C=	ENSP00000358872.4:p.Arg2022=
ENST00000422373.6:c.3161-407C=	ENSP00000416926.2:n.3161-407C=
ENST00000610817.5:c.6202C=	ENSP00000480593.2:n.6202C=
ENST00000673639.2:c.280-4392C=
ENST00000676696.1:c.6424C=	ENSP00000503392.1:n.6424C=
ENST00000678304.1:n.1324C=
ENST00000344736.8:c.6025C=	ENSP00000358863.3:p.Arg2009=
ENST00000360319.8:c.6121C=	ENSP00000353467.4:p.Arg2041=
ENST00000369850.7:c.6145C=	ENSP00000358866.3:p.Arg2049=
ENST00000369856.7:c.6064C=	ENSP00000358872.4:p.Arg2022=
ENST00000415241.1:c.347C=
ENST00000420627.5:c.6101C=	ENSP00000408921.1:n.6101C=
ENST00000422373.5:c.6121C=	ENSP00000416926.1:p.Arg2041=
ENST00000444578.1:c.88C=	ENSP00000397824.1:p.Arg30=
ENST00000466325.1:n.284C=
ENST00000490936.5:n.2134C=
ENST00000610817.4:c.5844+311C=	ENSP00000480593.1:n.5844+311C=
NM_001110556.1:c.6145C=	NP_001104026.1:p.Arg2049=
NM_001456.3:c.6121C=	NP_001447.2:p.Arg2041=
XM_011531127.1:c.6049C=	XP_011529429.1:p.Arg2017=
XM_011531128.1:c.6025C=	XP_011529430.1:p.Arg2009=
XM_011531129.1:c.5971C=	XP_011529431.1:p.Arg1991=
XM_011531130.1:c.5947C=	XP_011529432.1:p.Arg1983=
XM_011531131.1:c.5944C=	XP_011529433.1:p.Arg1982=
NM_001110556.2:c.6145C= MANE Select	NP_001104026.1:p.Arg2049=
NM_001456.4:c.6121C=	NP_001447.2:p.Arg2041=