Canonical Allele Identifier: CA2466653078

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352816C= , CM000685.2:g.154352816C=	GRCh38
NC_000023.10:g.153581184C= , CM000685.1:g.153581184C=	GRCh37
NC_000023.9:g.153234378C=	NCBI36
NG_011506.1:g.26823G=
NG_011506.2:g.26823G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6311G=	ENSP00000353467.4:p.Gly2104=
ENST00000369850.10:c.6335G= MANE Select	ENSP00000358866.3:p.Gly2112=
ENST00000369856.8:c.6254G=	ENSP00000358872.4:p.Gly2085=
ENST00000422373.6:c.3161-141G=	ENSP00000416926.2:n.3161-141G=
ENST00000610817.5:c.6392G=	ENSP00000480593.2:n.6392G=
ENST00000673639.2:c.280-4126G=
ENST00000676696.1:c.6614G=	ENSP00000503392.1:n.6614G=
ENST00000678304.1:n.1514G=
ENST00000344736.8:c.6215G=	ENSP00000358863.3:p.Gly2072=
ENST00000360319.8:c.6311G=	ENSP00000353467.4:p.Gly2104=
ENST00000369850.7:c.6335G=	ENSP00000358866.3:p.Gly2112=
ENST00000369856.7:c.6254G=	ENSP00000358872.4:p.Gly2085=
ENST00000415241.1:c.537G=
ENST00000420627.5:c.6291G=	ENSP00000408921.1:n.6291G=
ENST00000422373.5:c.6311G=	ENSP00000416926.1:p.Gly2104=
ENST00000444578.1:c.278G=	ENSP00000397824.1:p.Gly93=
ENST00000466325.1:n.550G=
ENST00000490936.5:n.2324G=
ENST00000498411.1:n.67+1G=
ENST00000610817.4:c.5844+577G=	ENSP00000480593.1:n.5844+577G=
NM_001110556.1:c.6335G=	NP_001104026.1:p.Gly2112=
NM_001456.3:c.6311G=	NP_001447.2:p.Gly2104=
XM_011531127.1:c.6239G=	XP_011529429.1:p.Gly2080=
XM_011531128.1:c.6215G=	XP_011529430.1:p.Gly2072=
XM_011531129.1:c.6161G=	XP_011529431.1:p.Gly2054=
XM_011531130.1:c.6137G=	XP_011529432.1:p.Gly2046=
XM_011531131.1:c.6134G=	XP_011529433.1:p.Gly2045=
NM_001110556.2:c.6335G= MANE Select	NP_001104026.1:p.Gly2112=
NM_001456.4:c.6311G=	NP_001447.2:p.Gly2104=