Canonical Allele Identifier: CA415193677

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581206T>A (hg19) ; chrX:g.154352838T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352838T>A , CM000685.2:g.154352838T>A	GRCh38
NC_000023.10:g.153581206T>A , CM000685.1:g.153581206T>A	GRCh37
NC_000023.9:g.153234400T>A	NCBI36
NG_011506.1:g.26801A>T
NG_011506.2:g.26801A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6289A>T	ENSP00000353467.4:p.Thr2097Ser
ENST00000369850.10:c.6313A>T MANE Select	ENSP00000358866.3:p.Thr2105Ser
ENST00000369856.8:c.6232A>T	ENSP00000358872.4:p.Thr2078Ser
ENST00000422373.6:c.3161-163A>T	ENSP00000416926.2:n.3161-163A>T
ENST00000610817.5:c.6370A>T	ENSP00000480593.2:n.6370A>T
ENST00000673639.2:c.280-4148A>T
ENST00000676696.1:c.6592A>T	ENSP00000503392.1:n.6592A>T
ENST00000678304.1:n.1492A>T
ENST00000344736.8:c.6193A>T	ENSP00000358863.3:p.Thr2065Ser
ENST00000360319.8:c.6289A>T	ENSP00000353467.4:p.Thr2097Ser
ENST00000369850.7:c.6313A>T	ENSP00000358866.3:p.Thr2105Ser
ENST00000369856.7:c.6232A>T	ENSP00000358872.4:p.Thr2078Ser
ENST00000415241.1:c.515A>T
ENST00000420627.5:c.6269A>T	ENSP00000408921.1:n.6269A>T
ENST00000422373.5:c.6289A>T	ENSP00000416926.1:p.Thr2097Ser
ENST00000444578.1:c.256A>T	ENSP00000397824.1:p.Thr86Ser
ENST00000466325.1:n.528A>T
ENST00000490936.5:n.2302A>T
ENST00000498411.1:n.46A>T
ENST00000610817.4:c.5844+555A>T	ENSP00000480593.1:n.5844+555A>T
NM_001110556.1:c.6313A>T	NP_001104026.1:p.Thr2105Ser
NM_001456.3:c.6289A>T	NP_001447.2:p.Thr2097Ser
XM_011531127.1:c.6217A>T	XP_011529429.1:p.Thr2073Ser
XM_011531128.1:c.6193A>T	XP_011529430.1:p.Thr2065Ser
XM_011531129.1:c.6139A>T	XP_011529431.1:p.Thr2047Ser
XM_011531130.1:c.6115A>T	XP_011529432.1:p.Thr2039Ser
XM_011531131.1:c.6112A>T	XP_011529433.1:p.Thr2038Ser
NM_001110556.2:c.6313A>T MANE Select	NP_001104026.1:p.Thr2105Ser
NM_001456.4:c.6289A>T	NP_001447.2:p.Thr2097Ser