Canonical Allele Identifier: CA2466653294

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353361G= , CM000685.2:g.154353361G=	GRCh38
NC_000023.10:g.153581729G= , CM000685.1:g.153581729G=	GRCh37
NC_000023.9:g.153234923G=	NCBI36
NG_011506.1:g.26278C=
NG_011506.2:g.26278C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5933C=	ENSP00000353467.4:p.Thr1978=
ENST00000369850.10:c.5957C= MANE Select	ENSP00000358866.3:p.Thr1986=
ENST00000369856.8:c.5876C=	ENSP00000358872.4:p.Thr1959=
ENST00000422373.6:c.3161-686C=	ENSP00000416926.2:n.3161-686C=
ENST00000610817.5:c.6014C=	ENSP00000480593.2:n.6014C=
ENST00000673639.2:c.280-4671C=
ENST00000676696.1:c.6236C=	ENSP00000503392.1:n.6236C=
ENST00000678304.1:n.1136C=
ENST00000344736.8:c.5837C=	ENSP00000358863.3:p.Thr1946=
ENST00000360319.8:c.5933C=	ENSP00000353467.4:p.Thr1978=
ENST00000369850.7:c.5957C=	ENSP00000358866.3:p.Thr1986=
ENST00000369856.7:c.5876C=	ENSP00000358872.4:p.Thr1959=
ENST00000415241.1:c.142C=
ENST00000420627.5:c.5913C=	ENSP00000408921.1:n.5913C=
ENST00000422373.5:c.5933C=	ENSP00000416926.1:p.Thr1978=
ENST00000438732.2:c.631C=
ENST00000466325.1:n.96C=
ENST00000490936.5:n.1946C=
ENST00000610817.4:c.5844+32C=	ENSP00000480593.1:n.5844+32C=
NM_001110556.1:c.5957C=	NP_001104026.1:p.Thr1986=
NM_001456.3:c.5933C=	NP_001447.2:p.Thr1978=
XM_011531127.1:c.5861C=	XP_011529429.1:p.Thr1954=
XM_011531128.1:c.5837C=	XP_011529430.1:p.Thr1946=
XM_011531129.1:c.5783C=	XP_011529431.1:p.Thr1928=
XM_011531130.1:c.5759C=	XP_011529432.1:p.Thr1920=
XM_011531131.1:c.5756C=	XP_011529433.1:p.Thr1919=
NM_001110556.2:c.5957C= MANE Select	NP_001104026.1:p.Thr1986=
NM_001456.4:c.5933C=	NP_001447.2:p.Thr1978=