Canonical Allele Identifier: CA2466653094

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352853C= , CM000685.2:g.154352853C=	GRCh38
NC_000023.10:g.153581221C= , CM000685.1:g.153581221C=	GRCh37
NC_000023.9:g.153234415C=	NCBI36
NG_011506.1:g.26786G=
NG_011506.2:g.26786G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6274G=	ENSP00000353467.4:p.Gly2092=
ENST00000369850.10:c.6298G= MANE Select	ENSP00000358866.3:p.Gly2100=
ENST00000369856.8:c.6217G=	ENSP00000358872.4:p.Gly2073=
ENST00000422373.6:c.3161-178G=	ENSP00000416926.2:n.3161-178G=
ENST00000610817.5:c.6355G=	ENSP00000480593.2:n.6355G=
ENST00000673639.2:c.280-4163G=
ENST00000676696.1:c.6577G=	ENSP00000503392.1:n.6577G=
ENST00000678304.1:n.1477G=
ENST00000344736.8:c.6178G=	ENSP00000358863.3:p.Gly2060=
ENST00000360319.8:c.6274G=	ENSP00000353467.4:p.Gly2092=
ENST00000369850.7:c.6298G=	ENSP00000358866.3:p.Gly2100=
ENST00000369856.7:c.6217G=	ENSP00000358872.4:p.Gly2073=
ENST00000415241.1:c.500G=
ENST00000420627.5:c.6254G=	ENSP00000408921.1:n.6254G=
ENST00000422373.5:c.6274G=	ENSP00000416926.1:p.Gly2092=
ENST00000444578.1:c.241G=	ENSP00000397824.1:p.Gly81=
ENST00000466325.1:n.513G=
ENST00000490936.5:n.2287G=
ENST00000498411.1:n.31G=
ENST00000610817.4:c.5844+540G=	ENSP00000480593.1:n.5844+540G=
NM_001110556.1:c.6298G=	NP_001104026.1:p.Gly2100=
NM_001456.3:c.6274G=	NP_001447.2:p.Gly2092=
XM_011531127.1:c.6202G=	XP_011529429.1:p.Gly2068=
XM_011531128.1:c.6178G=	XP_011529430.1:p.Gly2060=
XM_011531129.1:c.6124G=	XP_011529431.1:p.Gly2042=
XM_011531130.1:c.6100G=	XP_011529432.1:p.Gly2034=
XM_011531131.1:c.6097G=	XP_011529433.1:p.Gly2033=
NM_001110556.2:c.6298G= MANE Select	NP_001104026.1:p.Gly2100=
NM_001456.4:c.6274G=	NP_001447.2:p.Gly2092=