Canonical Allele Identifier: CA2466653226

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353177C= , CM000685.2:g.154353177C=	GRCh38
NC_000023.10:g.153581545C= , CM000685.1:g.153581545C=	GRCh37
NC_000023.9:g.153234739C=	NCBI36
NG_011506.1:g.26462G=
NG_011506.2:g.26462G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6026G=	ENSP00000353467.4:p.Gly2009=
ENST00000369850.10:c.6050G= MANE Select	ENSP00000358866.3:p.Gly2017=
ENST00000369856.8:c.5969G=	ENSP00000358872.4:p.Gly1990=
ENST00000422373.6:c.3161-502G=	ENSP00000416926.2:n.3161-502G=
ENST00000610817.5:c.6107G=	ENSP00000480593.2:n.6107G=
ENST00000673639.2:c.280-4487G=
ENST00000676696.1:c.6329G=	ENSP00000503392.1:n.6329G=
ENST00000678304.1:n.1229G=
ENST00000344736.8:c.5930G=	ENSP00000358863.3:p.Gly1977=
ENST00000360319.8:c.6026G=	ENSP00000353467.4:p.Gly2009=
ENST00000369850.7:c.6050G=	ENSP00000358866.3:p.Gly2017=
ENST00000369856.7:c.5969G=	ENSP00000358872.4:p.Gly1990=
ENST00000415241.1:c.252G=
ENST00000420627.5:c.6006G=	ENSP00000408921.1:n.6006G=
ENST00000422373.5:c.6026G=	ENSP00000416926.1:p.Gly2009=
ENST00000466325.1:n.189G=
ENST00000490936.5:n.2039G=
ENST00000610817.4:c.5844+216G=	ENSP00000480593.1:n.5844+216G=
NM_001110556.1:c.6050G=	NP_001104026.1:p.Gly2017=
NM_001456.3:c.6026G=	NP_001447.2:p.Gly2009=
XM_011531127.1:c.5954G=	XP_011529429.1:p.Gly1985=
XM_011531128.1:c.5930G=	XP_011529430.1:p.Gly1977=
XM_011531129.1:c.5876G=	XP_011529431.1:p.Gly1959=
XM_011531130.1:c.5852G=	XP_011529432.1:p.Gly1951=
XM_011531131.1:c.5849G=	XP_011529433.1:p.Gly1950=
NM_001110556.2:c.6050G= MANE Select	NP_001104026.1:p.Gly2017=
NM_001456.4:c.6026G=	NP_001447.2:p.Gly2009=