Canonical Allele Identifier: CA519706529

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153580997C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352629C>T , CM000685.2:g.154352629C>T	GRCh38
NC_000023.10:g.153580997C>T , CM000685.1:g.153580997C>T	GRCh37
NC_000023.9:g.153234191C>T	NCBI36
NG_011506.1:g.27010G>A
NG_011506.2:g.27010G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6402G>A	ENSP00000353467.4:p.Glu2134=
ENST00000369850.10:c.6426G>A MANE Select	ENSP00000358866.3:p.Glu2142=
ENST00000369856.8:c.6345G>A	ENSP00000358872.4:p.Glu2115=
ENST00000422373.6:c.3207G>A	ENSP00000416926.2:p.Glu1069=
ENST00000610817.5:c.6483G>A	ENSP00000480593.2:n.6483G>A
ENST00000673639.2:c.280-3939G>A
ENST00000676696.1:c.6705G>A	ENSP00000503392.1:n.6705G>A
ENST00000678304.1:n.1605G>A
ENST00000344736.8:c.6306G>A	ENSP00000358863.3:p.Glu2102=
ENST00000360319.8:c.6402G>A	ENSP00000353467.4:p.Glu2134=
ENST00000369850.7:c.6426G>A	ENSP00000358866.3:p.Glu2142=
ENST00000369856.7:c.6345G>A	ENSP00000358872.4:p.Glu2115=
ENST00000415241.1:c.628G>A
ENST00000420627.5:c.6382G>A	ENSP00000408921.1:n.6382G>A
ENST00000422373.5:c.6402G>A	ENSP00000416926.1:p.Glu2134=
ENST00000444578.1:c.322+143G>A	ENSP00000397824.1:n.322+143G>A
ENST00000466325.1:n.737G>A
ENST00000474358.5:n.59G>A
ENST00000490936.5:n.2415G>A
ENST00000498411.1:n.67+188G>A
ENST00000610817.4:c.5845-679G>A	ENSP00000480593.1:n.5845-679G>A
NM_001110556.1:c.6426G>A	NP_001104026.1:p.Glu2142=
NM_001456.3:c.6402G>A	NP_001447.2:p.Glu2134=
XM_011531127.1:c.6330G>A	XP_011529429.1:p.Glu2110=
XM_011531128.1:c.6306G>A	XP_011529430.1:p.Glu2102=
XM_011531129.1:c.6252G>A	XP_011529431.1:p.Glu2084=
XM_011531130.1:c.6228G>A	XP_011529432.1:p.Glu2076=
XM_011531131.1:c.6225G>A	XP_011529433.1:p.Glu2075=
NM_001110556.2:c.6426G>A MANE Select	NP_001104026.1:p.Glu2142=
NM_001456.4:c.6402G>A	NP_001447.2:p.Glu2134=