Canonical Allele Identifier: CA2466653114

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352905C= , CM000685.2:g.154352905C=	GRCh38
NC_000023.10:g.153581273C= , CM000685.1:g.153581273C=	GRCh37
NC_000023.9:g.153234467C=	NCBI36
NG_011506.1:g.26734G=
NG_011506.2:g.26734G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6222G=	ENSP00000353467.4:p.Leu2074=
ENST00000369850.10:c.6246G= MANE Select	ENSP00000358866.3:p.Leu2082=
ENST00000369856.8:c.6165G=	ENSP00000358872.4:p.Leu2055=
ENST00000422373.6:c.3161-230G=	ENSP00000416926.2:n.3161-230G=
ENST00000610817.5:c.6303G=	ENSP00000480593.2:n.6303G=
ENST00000673639.2:c.280-4215G=
ENST00000676696.1:c.6525G=	ENSP00000503392.1:n.6525G=
ENST00000678304.1:n.1425G=
ENST00000344736.8:c.6126G=	ENSP00000358863.3:p.Leu2042=
ENST00000360319.8:c.6222G=	ENSP00000353467.4:p.Leu2074=
ENST00000369850.7:c.6246G=	ENSP00000358866.3:p.Leu2082=
ENST00000369856.7:c.6165G=	ENSP00000358872.4:p.Leu2055=
ENST00000415241.1:c.448G=
ENST00000420627.5:c.6202G=	ENSP00000408921.1:n.6202G=
ENST00000422373.5:c.6222G=	ENSP00000416926.1:p.Leu2074=
ENST00000444578.1:c.189G=	ENSP00000397824.1:p.Leu63=
ENST00000466325.1:n.461G=
ENST00000490936.5:n.2235G=
ENST00000610817.4:c.5844+488G=	ENSP00000480593.1:n.5844+488G=
NM_001110556.1:c.6246G=	NP_001104026.1:p.Leu2082=
NM_001456.3:c.6222G=	NP_001447.2:p.Leu2074=
XM_011531127.1:c.6150G=	XP_011529429.1:p.Leu2050=
XM_011531128.1:c.6126G=	XP_011529430.1:p.Leu2042=
XM_011531129.1:c.6072G=	XP_011529431.1:p.Leu2024=
XM_011531130.1:c.6048G=	XP_011529432.1:p.Leu2016=
XM_011531131.1:c.6045G=	XP_011529433.1:p.Leu2015=
NM_001110556.2:c.6246G= MANE Select	NP_001104026.1:p.Leu2082=
NM_001456.4:c.6222G=	NP_001447.2:p.Leu2074=