Canonical Allele Identifier: CA519706109

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581237T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352869T>G , CM000685.2:g.154352869T>G	GRCh38
NC_000023.10:g.153581237T>G , CM000685.1:g.153581237T>G	GRCh37
NC_000023.9:g.153234431T>G	NCBI36
NG_011506.1:g.26770A>C
NG_011506.2:g.26770A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6258A>C	ENSP00000353467.4:p.Thr2086=
ENST00000369850.10:c.6282A>C MANE Select	ENSP00000358866.3:p.Thr2094=
ENST00000369856.8:c.6201A>C	ENSP00000358872.4:p.Thr2067=
ENST00000422373.6:c.3161-194A>C	ENSP00000416926.2:n.3161-194A>C
ENST00000610817.5:c.6339A>C	ENSP00000480593.2:n.6339A>C
ENST00000673639.2:c.280-4179A>C
ENST00000676696.1:c.6561A>C	ENSP00000503392.1:n.6561A>C
ENST00000678304.1:n.1461A>C
ENST00000344736.8:c.6162A>C	ENSP00000358863.3:p.Thr2054=
ENST00000360319.8:c.6258A>C	ENSP00000353467.4:p.Thr2086=
ENST00000369850.7:c.6282A>C	ENSP00000358866.3:p.Thr2094=
ENST00000369856.7:c.6201A>C	ENSP00000358872.4:p.Thr2067=
ENST00000415241.1:c.484A>C
ENST00000420627.5:c.6238A>C	ENSP00000408921.1:n.6238A>C
ENST00000422373.5:c.6258A>C	ENSP00000416926.1:p.Thr2086=
ENST00000444578.1:c.225A>C	ENSP00000397824.1:p.Thr75=
ENST00000466325.1:n.497A>C
ENST00000490936.5:n.2271A>C
ENST00000498411.1:n.15A>C
ENST00000610817.4:c.5844+524A>C	ENSP00000480593.1:n.5844+524A>C
NM_001110556.1:c.6282A>C	NP_001104026.1:p.Thr2094=
NM_001456.3:c.6258A>C	NP_001447.2:p.Thr2086=
XM_011531127.1:c.6186A>C	XP_011529429.1:p.Thr2062=
XM_011531128.1:c.6162A>C	XP_011529430.1:p.Thr2054=
XM_011531129.1:c.6108A>C	XP_011529431.1:p.Thr2036=
XM_011531130.1:c.6084A>C	XP_011529432.1:p.Thr2028=
XM_011531131.1:c.6081A>C	XP_011529433.1:p.Thr2027=
NM_001110556.2:c.6282A>C MANE Select	NP_001104026.1:p.Thr2094=
NM_001456.4:c.6258A>C	NP_001447.2:p.Thr2086=