Canonical Allele Identifier: CA2466653069

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352791A= , CM000685.2:g.154352791A=	GRCh38
NC_000023.10:g.153581159A= , CM000685.1:g.153581159A=	GRCh37
NC_000023.9:g.153234353A=	NCBI36
NG_011506.1:g.26848T=
NG_011506.2:g.26848T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6336T=	ENSP00000353467.4:p.Phe2112=
ENST00000369850.10:c.6360T= MANE Select	ENSP00000358866.3:p.Phe2120=
ENST00000369856.8:c.6279T=	ENSP00000358872.4:p.Phe2093=
ENST00000422373.6:c.3161-116T=	ENSP00000416926.2:n.3161-116T=
ENST00000610817.5:c.6417T=	ENSP00000480593.2:n.6417T=
ENST00000673639.2:c.280-4101T=
ENST00000676696.1:c.6639T=	ENSP00000503392.1:n.6639T=
ENST00000678304.1:n.1539T=
ENST00000344736.8:c.6240T=	ENSP00000358863.3:p.Phe2080=
ENST00000360319.8:c.6336T=	ENSP00000353467.4:p.Phe2112=
ENST00000369850.7:c.6360T=	ENSP00000358866.3:p.Phe2120=
ENST00000369856.7:c.6279T=	ENSP00000358872.4:p.Phe2093=
ENST00000415241.1:c.562T=
ENST00000420627.5:c.6316T=	ENSP00000408921.1:n.6316T=
ENST00000422373.5:c.6336T=	ENSP00000416926.1:p.Phe2112=
ENST00000444578.1:c.303T=	ENSP00000397824.1:p.Phe101=
ENST00000466325.1:n.575T=
ENST00000490936.5:n.2349T=
ENST00000498411.1:n.67+26T=
ENST00000610817.4:c.5844+602T=	ENSP00000480593.1:n.5844+602T=
NM_001110556.1:c.6360T=	NP_001104026.1:p.Phe2120=
NM_001456.3:c.6336T=	NP_001447.2:p.Phe2112=
XM_011531127.1:c.6264T=	XP_011529429.1:p.Phe2088=
XM_011531128.1:c.6240T=	XP_011529430.1:p.Phe2080=
XM_011531129.1:c.6186T=	XP_011529431.1:p.Phe2062=
XM_011531130.1:c.6162T=	XP_011529432.1:p.Phe2054=
XM_011531131.1:c.6159T=	XP_011529433.1:p.Phe2053=
NM_001110556.2:c.6360T= MANE Select	NP_001104026.1:p.Phe2120=
NM_001456.4:c.6336T=	NP_001447.2:p.Phe2112=