Canonical Allele Identifier: CA415196452

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581533A>T (hg19) ; chrX:g.154353165A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353165A>T , CM000685.2:g.154353165A>T	GRCh38
NC_000023.10:g.153581533A>T , CM000685.1:g.153581533A>T	GRCh37
NC_000023.9:g.153234727A>T	NCBI36
NG_011506.1:g.26474T>A
NG_011506.2:g.26474T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6038T>A	ENSP00000353467.4:p.Val2013Glu
ENST00000369850.10:c.6062T>A MANE Select	ENSP00000358866.3:p.Val2021Glu
ENST00000369856.8:c.5981T>A	ENSP00000358872.4:p.Val1994Glu
ENST00000422373.6:c.3161-490T>A	ENSP00000416926.2:n.3161-490T>A
ENST00000610817.5:c.6119T>A	ENSP00000480593.2:n.6119T>A
ENST00000673639.2:c.280-4475T>A
ENST00000676696.1:c.6341T>A	ENSP00000503392.1:n.6341T>A
ENST00000678304.1:n.1241T>A
ENST00000344736.8:c.5942T>A	ENSP00000358863.3:p.Val1981Glu
ENST00000360319.8:c.6038T>A	ENSP00000353467.4:p.Val2013Glu
ENST00000369850.7:c.6062T>A	ENSP00000358866.3:p.Val2021Glu
ENST00000369856.7:c.5981T>A	ENSP00000358872.4:p.Val1994Glu
ENST00000415241.1:c.264T>A
ENST00000420627.5:c.6018T>A	ENSP00000408921.1:n.6018T>A
ENST00000422373.5:c.6038T>A	ENSP00000416926.1:p.Val2013Glu
ENST00000444578.1:c.5T>A	ENSP00000397824.1:p.Val2Glu
ENST00000466325.1:n.201T>A
ENST00000490936.5:n.2051T>A
ENST00000610817.4:c.5844+228T>A	ENSP00000480593.1:n.5844+228T>A
NM_001110556.1:c.6062T>A	NP_001104026.1:p.Val2021Glu
NM_001456.3:c.6038T>A	NP_001447.2:p.Val2013Glu
XM_011531127.1:c.5966T>A	XP_011529429.1:p.Val1989Glu
XM_011531128.1:c.5942T>A	XP_011529430.1:p.Val1981Glu
XM_011531129.1:c.5888T>A	XP_011529431.1:p.Val1963Glu
XM_011531130.1:c.5864T>A	XP_011529432.1:p.Val1955Glu
XM_011531131.1:c.5861T>A	XP_011529433.1:p.Val1954Glu
NM_001110556.2:c.6062T>A MANE Select	NP_001104026.1:p.Val2021Glu
NM_001456.4:c.6038T>A	NP_001447.2:p.Val2013Glu