Canonical Allele Identifier: CA2466653165

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353018A= , CM000685.2:g.154353018A=	GRCh38
NC_000023.10:g.153581386A= , CM000685.1:g.153581386A=	GRCh37
NC_000023.9:g.153234580A=	NCBI36
NG_011506.1:g.26621T=
NG_011506.2:g.26621T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6185T=	ENSP00000353467.4:p.Ile2062=
ENST00000369850.10:c.6209T= MANE Select	ENSP00000358866.3:p.Ile2070=
ENST00000369856.8:c.6128T=	ENSP00000358872.4:p.Ile2043=
ENST00000422373.6:c.3161-343T=	ENSP00000416926.2:n.3161-343T=
ENST00000610817.5:c.6266T=	ENSP00000480593.2:n.6266T=
ENST00000673639.2:c.280-4328T=
ENST00000676696.1:c.6488T=	ENSP00000503392.1:n.6488T=
ENST00000678304.1:n.1388T=
ENST00000344736.8:c.6089T=	ENSP00000358863.3:p.Ile2030=
ENST00000360319.8:c.6185T=	ENSP00000353467.4:p.Ile2062=
ENST00000369850.7:c.6209T=	ENSP00000358866.3:p.Ile2070=
ENST00000369856.7:c.6128T=	ENSP00000358872.4:p.Ile2043=
ENST00000415241.1:c.411T=
ENST00000420627.5:c.6165T=	ENSP00000408921.1:n.6165T=
ENST00000422373.5:c.6185T=	ENSP00000416926.1:p.Ile2062=
ENST00000444578.1:c.152T=	ENSP00000397824.1:p.Ile51=
ENST00000466325.1:n.348T=
ENST00000490936.5:n.2198T=
ENST00000610817.4:c.5844+375T=	ENSP00000480593.1:n.5844+375T=
NM_001110556.1:c.6209T=	NP_001104026.1:p.Ile2070=
NM_001456.3:c.6185T=	NP_001447.2:p.Ile2062=
XM_011531127.1:c.6113T=	XP_011529429.1:p.Ile2038=
XM_011531128.1:c.6089T=	XP_011529430.1:p.Ile2030=
XM_011531129.1:c.6035T=	XP_011529431.1:p.Ile2012=
XM_011531130.1:c.6011T=	XP_011529432.1:p.Ile2004=
XM_011531131.1:c.6008T=	XP_011529433.1:p.Ile2003=
NM_001110556.2:c.6209T= MANE Select	NP_001104026.1:p.Ile2070=
NM_001456.4:c.6185T=	NP_001447.2:p.Ile2062=