Canonical Allele Identifier: CA2466653233

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353199A= , CM000685.2:g.154353199A=	GRCh38
NC_000023.10:g.153581567A= , CM000685.1:g.153581567A=	GRCh37
NC_000023.9:g.153234761A=	NCBI36
NG_011506.1:g.26440T=
NG_011506.2:g.26440T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6004T=	ENSP00000353467.4:p.Ser2002=
ENST00000369850.10:c.6028T= MANE Select	ENSP00000358866.3:p.Ser2010=
ENST00000369856.8:c.5947T=	ENSP00000358872.4:p.Ser1983=
ENST00000422373.6:c.3161-524T=	ENSP00000416926.2:n.3161-524T=
ENST00000610817.5:c.6085T=	ENSP00000480593.2:n.6085T=
ENST00000673639.2:c.280-4509T=
ENST00000676696.1:c.6307T=	ENSP00000503392.1:n.6307T=
ENST00000678304.1:n.1207T=
ENST00000344736.8:c.5908T=	ENSP00000358863.3:p.Ser1970=
ENST00000360319.8:c.6004T=	ENSP00000353467.4:p.Ser2002=
ENST00000369850.7:c.6028T=	ENSP00000358866.3:p.Ser2010=
ENST00000369856.7:c.5947T=	ENSP00000358872.4:p.Ser1983=
ENST00000415241.1:c.230T=
ENST00000420627.5:c.5984T=	ENSP00000408921.1:n.5984T=
ENST00000422373.5:c.6004T=	ENSP00000416926.1:p.Ser2002=
ENST00000466325.1:n.167T=
ENST00000490936.5:n.2017T=
ENST00000610817.4:c.5844+194T=	ENSP00000480593.1:n.5844+194T=
NM_001110556.1:c.6028T=	NP_001104026.1:p.Ser2010=
NM_001456.3:c.6004T=	NP_001447.2:p.Ser2002=
XM_011531127.1:c.5932T=	XP_011529429.1:p.Ser1978=
XM_011531128.1:c.5908T=	XP_011529430.1:p.Ser1970=
XM_011531129.1:c.5854T=	XP_011529431.1:p.Ser1952=
XM_011531130.1:c.5830T=	XP_011529432.1:p.Ser1944=
XM_011531131.1:c.5827T=	XP_011529433.1:p.Ser1943=
NM_001110556.2:c.6028T= MANE Select	NP_001104026.1:p.Ser2010=
NM_001456.4:c.6004T=	NP_001447.2:p.Ser2002=