Canonical Allele Identifier: CA415193798

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581214C>T (hg19) ; chrX:g.154352846C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352846C>T , CM000685.2:g.154352846C>T	GRCh38
NC_000023.10:g.153581214C>T , CM000685.1:g.153581214C>T	GRCh37
NC_000023.9:g.153234408C>T	NCBI36
NG_011506.1:g.26793G>A
NG_011506.2:g.26793G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6281G>A	ENSP00000353467.4:p.Cys2094Tyr
ENST00000369850.10:c.6305G>A MANE Select	ENSP00000358866.3:p.Cys2102Tyr
ENST00000369856.8:c.6224G>A	ENSP00000358872.4:p.Cys2075Tyr
ENST00000422373.6:c.3161-171G>A	ENSP00000416926.2:n.3161-171G>A
ENST00000610817.5:c.6362G>A	ENSP00000480593.2:n.6362G>A
ENST00000673639.2:c.280-4156G>A
ENST00000676696.1:c.6584G>A	ENSP00000503392.1:n.6584G>A
ENST00000678304.1:n.1484G>A
ENST00000344736.8:c.6185G>A	ENSP00000358863.3:p.Cys2062Tyr
ENST00000360319.8:c.6281G>A	ENSP00000353467.4:p.Cys2094Tyr
ENST00000369850.7:c.6305G>A	ENSP00000358866.3:p.Cys2102Tyr
ENST00000369856.7:c.6224G>A	ENSP00000358872.4:p.Cys2075Tyr
ENST00000415241.1:c.507G>A
ENST00000420627.5:c.6261G>A	ENSP00000408921.1:n.6261G>A
ENST00000422373.5:c.6281G>A	ENSP00000416926.1:p.Cys2094Tyr
ENST00000444578.1:c.248G>A	ENSP00000397824.1:p.Cys83Tyr
ENST00000466325.1:n.520G>A
ENST00000490936.5:n.2294G>A
ENST00000498411.1:n.38G>A
ENST00000610817.4:c.5844+547G>A	ENSP00000480593.1:n.5844+547G>A
NM_001110556.1:c.6305G>A	NP_001104026.1:p.Cys2102Tyr
NM_001456.3:c.6281G>A	NP_001447.2:p.Cys2094Tyr
XM_011531127.1:c.6209G>A	XP_011529429.1:p.Cys2070Tyr
XM_011531128.1:c.6185G>A	XP_011529430.1:p.Cys2062Tyr
XM_011531129.1:c.6131G>A	XP_011529431.1:p.Cys2044Tyr
XM_011531130.1:c.6107G>A	XP_011529432.1:p.Cys2036Tyr
XM_011531131.1:c.6104G>A	XP_011529433.1:p.Cys2035Tyr
NM_001110556.2:c.6305G>A MANE Select	NP_001104026.1:p.Cys2102Tyr
NM_001456.4:c.6281G>A	NP_001447.2:p.Cys2094Tyr