Canonical Allele Identifier: CA415193806

Gene: FLNA

Linked Data

• gnomAD v4: X-154352846-C-A
• MyVariant Identifiers: chrX:g.153581214C>A (hg19) ; chrX:g.154352846C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6281G>T	ENSP00000353467.4:p.Cys2094Phe
ENST00000369850.10:c.6305G>T MANE Select	ENSP00000358866.3:p.Cys2102Phe
ENST00000369856.8:c.6224G>T	ENSP00000358872.4:p.Cys2075Phe
ENST00000422373.6:c.3161-171G>T	ENSP00000416926.2:n.3161-171G>T
ENST00000610817.5:c.6362G>T	ENSP00000480593.2:n.6362G>T
ENST00000673639.2:c.280-4156G>T
ENST00000676696.1:c.6584G>T	ENSP00000503392.1:n.6584G>T
ENST00000678304.1:n.1484G>T
ENST00000344736.8:c.6185G>T	ENSP00000358863.3:p.Cys2062Phe
ENST00000360319.8:c.6281G>T	ENSP00000353467.4:p.Cys2094Phe
ENST00000369850.7:c.6305G>T	ENSP00000358866.3:p.Cys2102Phe
ENST00000369856.7:c.6224G>T	ENSP00000358872.4:p.Cys2075Phe
ENST00000415241.1:c.507G>T
ENST00000420627.5:c.6261G>T	ENSP00000408921.1:n.6261G>T
ENST00000422373.5:c.6281G>T	ENSP00000416926.1:p.Cys2094Phe
ENST00000444578.1:c.248G>T	ENSP00000397824.1:p.Cys83Phe
ENST00000466325.1:n.520G>T
ENST00000490936.5:n.2294G>T
ENST00000498411.1:n.38G>T
ENST00000610817.4:c.5844+547G>T	ENSP00000480593.1:n.5844+547G>T
NM_001110556.1:c.6305G>T	NP_001104026.1:p.Cys2102Phe
NM_001456.3:c.6281G>T	NP_001447.2:p.Cys2094Phe
XM_011531127.1:c.6209G>T	XP_011529429.1:p.Cys2070Phe
XM_011531128.1:c.6185G>T	XP_011529430.1:p.Cys2062Phe
XM_011531129.1:c.6131G>T	XP_011529431.1:p.Cys2044Phe
XM_011531130.1:c.6107G>T	XP_011529432.1:p.Cys2036Phe
XM_011531131.1:c.6104G>T	XP_011529433.1:p.Cys2035Phe
NM_001110556.2:c.6305G>T MANE Select	NP_001104026.1:p.Cys2102Phe
NM_001456.4:c.6281G>T	NP_001447.2:p.Cys2094Phe