Canonical Allele Identifier: CA2466653088

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352837G= , CM000685.2:g.154352837G=	GRCh38
NC_000023.10:g.153581205G= , CM000685.1:g.153581205G=	GRCh37
NC_000023.9:g.153234399G=	NCBI36
NG_011506.1:g.26802C=
NG_011506.2:g.26802C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6290C=	ENSP00000353467.4:p.Thr2097=
ENST00000369850.10:c.6314C= MANE Select	ENSP00000358866.3:p.Thr2105=
ENST00000369856.8:c.6233C=	ENSP00000358872.4:p.Thr2078=
ENST00000422373.6:c.3161-162C=	ENSP00000416926.2:n.3161-162C=
ENST00000610817.5:c.6371C=	ENSP00000480593.2:n.6371C=
ENST00000673639.2:c.280-4147C=
ENST00000676696.1:c.6593C=	ENSP00000503392.1:n.6593C=
ENST00000678304.1:n.1493C=
ENST00000344736.8:c.6194C=	ENSP00000358863.3:p.Thr2065=
ENST00000360319.8:c.6290C=	ENSP00000353467.4:p.Thr2097=
ENST00000369850.7:c.6314C=	ENSP00000358866.3:p.Thr2105=
ENST00000369856.7:c.6233C=	ENSP00000358872.4:p.Thr2078=
ENST00000415241.1:c.516C=
ENST00000420627.5:c.6270C=	ENSP00000408921.1:n.6270C=
ENST00000422373.5:c.6290C=	ENSP00000416926.1:p.Thr2097=
ENST00000444578.1:c.257C=	ENSP00000397824.1:p.Thr86=
ENST00000466325.1:n.529C=
ENST00000490936.5:n.2303C=
ENST00000498411.1:n.47C=
ENST00000610817.4:c.5844+556C=	ENSP00000480593.1:n.5844+556C=
NM_001110556.1:c.6314C=	NP_001104026.1:p.Thr2105=
NM_001456.3:c.6290C=	NP_001447.2:p.Thr2097=
XM_011531127.1:c.6218C=	XP_011529429.1:p.Thr2073=
XM_011531128.1:c.6194C=	XP_011529430.1:p.Thr2065=
XM_011531129.1:c.6140C=	XP_011529431.1:p.Thr2047=
XM_011531130.1:c.6116C=	XP_011529432.1:p.Thr2039=
XM_011531131.1:c.6113C=	XP_011529433.1:p.Thr2038=
NM_001110556.2:c.6314C= MANE Select	NP_001104026.1:p.Thr2105=
NM_001456.4:c.6290C=	NP_001447.2:p.Thr2097=