Canonical Allele Identifier: CA2466653264

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353279A= , CM000685.2:g.154353279A=	GRCh38
NC_000023.10:g.153581647A= , CM000685.1:g.153581647A=	GRCh37
NC_000023.9:g.153234841A=	NCBI36
NG_011506.1:g.26360T=
NG_011506.2:g.26360T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5998+17T=	ENSP00000353467.4:n.5998+17T=
ENST00000369850.10:c.6022+17T= MANE Select	ENSP00000358866.3:n.6022+17T=
ENST00000369856.8:c.5941+17T=	ENSP00000358872.4:n.5941+17T=
ENST00000422373.6:c.3161-604T=	ENSP00000416926.2:n.3161-604T=
ENST00000610817.5:c.6079+17T=	ENSP00000480593.2:n.6079+17T=
ENST00000673639.2:c.280-4589T=
ENST00000676696.1:c.6301+17T=	ENSP00000503392.1:n.6301+17T=
ENST00000678304.1:n.1201+17T=
ENST00000344736.8:c.5902+17T=	ENSP00000358863.3:n.5902+17T=
ENST00000360319.8:c.5998+17T=	ENSP00000353467.4:n.5998+17T=
ENST00000369850.7:c.6022+17T=	ENSP00000358866.3:n.6022+17T=
ENST00000369856.7:c.5941+17T=	ENSP00000358872.4:n.5941+17T=
ENST00000415241.1:c.207+17T=
ENST00000420627.5:c.5978+17T=	ENSP00000408921.1:n.5978+17T=
ENST00000422373.5:c.5998+17T=	ENSP00000416926.1:n.5998+17T=
ENST00000466325.1:n.161+17T=
ENST00000490936.5:n.2011+17T=
ENST00000610817.4:c.5844+114T=	ENSP00000480593.1:n.5844+114T=
NM_001110556.1:c.6022+17T=	NP_001104026.1:n.6022+17T=
NM_001456.3:c.5998+17T=	NP_001447.2:n.5998+17T=
XM_011531127.1:c.5926+17T=	XP_011529429.1:n.5926+17T=
XM_011531128.1:c.5902+17T=	XP_011529430.1:n.5902+17T=
XM_011531129.1:c.5848+17T=	XP_011529431.1:n.5848+17T=
XM_011531130.1:c.5824+17T=	XP_011529432.1:n.5824+17T=
XM_011531131.1:c.5821+17T=	XP_011529433.1:n.5821+17T=
NM_001110556.2:c.6022+17T= MANE Select	NP_001104026.1:n.6022+17T=
NM_001456.4:c.5998+17T=	NP_001447.2:n.5998+17T=