Canonical Allele Identifier: CA519706517

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153580988G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352620G>C , CM000685.2:g.154352620G>C	GRCh38
NC_000023.10:g.153580988G>C , CM000685.1:g.153580988G>C	GRCh37
NC_000023.9:g.153234182G>C	NCBI36
NG_011506.1:g.27019C>G
NG_011506.2:g.27019C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6411C>G	ENSP00000353467.4:p.Thr2137=
ENST00000369850.10:c.6435C>G MANE Select	ENSP00000358866.3:p.Thr2145=
ENST00000369856.8:c.6354C>G	ENSP00000358872.4:p.Thr2118=
ENST00000422373.6:c.3216C>G	ENSP00000416926.2:p.Thr1072=
ENST00000610817.5:c.6492C>G	ENSP00000480593.2:n.6492C>G
ENST00000673639.2:c.280-3930C>G
ENST00000676696.1:c.6714C>G	ENSP00000503392.1:n.6714C>G
ENST00000678304.1:n.1614C>G
ENST00000344736.8:c.6315C>G	ENSP00000358863.3:p.Thr2105=
ENST00000360319.8:c.6411C>G	ENSP00000353467.4:p.Thr2137=
ENST00000369850.7:c.6435C>G	ENSP00000358866.3:p.Thr2145=
ENST00000369856.7:c.6354C>G	ENSP00000358872.4:p.Thr2118=
ENST00000415241.1:c.637C>G
ENST00000420627.5:c.6391C>G	ENSP00000408921.1:n.6391C>G
ENST00000422373.5:c.6411C>G	ENSP00000416926.1:p.Thr2137=
ENST00000444578.1:c.322+152C>G	ENSP00000397824.1:n.322+152C>G
ENST00000466325.1:n.746C>G
ENST00000474358.5:n.68C>G
ENST00000490936.5:n.2424C>G
ENST00000498411.1:n.67+197C>G
ENST00000610817.4:c.5845-670C>G	ENSP00000480593.1:n.5845-670C>G
NM_001110556.1:c.6435C>G	NP_001104026.1:p.Thr2145=
NM_001456.3:c.6411C>G	NP_001447.2:p.Thr2137=
XM_011531127.1:c.6339C>G	XP_011529429.1:p.Thr2113=
XM_011531128.1:c.6315C>G	XP_011529430.1:p.Thr2105=
XM_011531129.1:c.6261C>G	XP_011529431.1:p.Thr2087=
XM_011531130.1:c.6237C>G	XP_011529432.1:p.Thr2079=
XM_011531131.1:c.6234C>G	XP_011529433.1:p.Thr2078=
NM_001110556.2:c.6435C>G MANE Select	NP_001104026.1:p.Thr2145=
NM_001456.4:c.6411C>G	NP_001447.2:p.Thr2137=