Canonical Allele Identifier: CA10560197

Gene: FLNA

Linked Data

• dbSNP Id: rs781888305
• ExAC: X:153581730 T / C
• gnomAD v2: X-153581730-T-C
• MyVariant Identifiers: chrX:g.153581730T>C (hg19) ; chrX:g.154353362T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353362T>C , CM000685.2:g.154353362T>C	GRCh38
NC_000023.10:g.153581730T>C , CM000685.1:g.153581730T>C	GRCh37
NC_000023.9:g.153234924T>C	NCBI36
NG_011506.1:g.26277A>G
NG_011506.2:g.26277A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5932A>G	ENSP00000353467.4:p.Thr1978Ala
ENST00000369850.10:c.5956A>G MANE Select	ENSP00000358866.3:p.Thr1986Ala
ENST00000369856.8:c.5875A>G	ENSP00000358872.4:p.Thr1959Ala
ENST00000422373.6:c.3161-687A>G	ENSP00000416926.2:n.3161-687A>G
ENST00000610817.5:c.6013A>G	ENSP00000480593.2:n.6013A>G
ENST00000673639.2:c.280-4672A>G
ENST00000676696.1:c.6235A>G	ENSP00000503392.1:n.6235A>G
ENST00000678304.1:n.1135A>G
ENST00000344736.8:c.5836A>G	ENSP00000358863.3:p.Thr1946Ala
ENST00000360319.8:c.5932A>G	ENSP00000353467.4:p.Thr1978Ala
ENST00000369850.7:c.5956A>G	ENSP00000358866.3:p.Thr1986Ala
ENST00000369856.7:c.5875A>G	ENSP00000358872.4:p.Thr1959Ala
ENST00000415241.1:c.141A>G
ENST00000420627.5:c.5912A>G	ENSP00000408921.1:n.5912A>G
ENST00000422373.5:c.5932A>G	ENSP00000416926.1:p.Thr1978Ala
ENST00000438732.2:c.630A>G
ENST00000466325.1:n.95A>G
ENST00000490936.5:n.1945A>G
ENST00000610817.4:c.5844+31A>G	ENSP00000480593.1:n.5844+31A>G
NM_001110556.1:c.5956A>G	NP_001104026.1:p.Thr1986Ala
NM_001456.3:c.5932A>G	NP_001447.2:p.Thr1978Ala
XM_011531127.1:c.5860A>G	XP_011529429.1:p.Thr1954Ala
XM_011531128.1:c.5836A>G	XP_011529430.1:p.Thr1946Ala
XM_011531129.1:c.5782A>G	XP_011529431.1:p.Thr1928Ala
XM_011531130.1:c.5758A>G	XP_011529432.1:p.Thr1920Ala
XM_011531131.1:c.5755A>G	XP_011529433.1:p.Thr1919Ala
NM_001110556.2:c.5956A>G MANE Select	NP_001104026.1:p.Thr1986Ala
NM_001456.4:c.5932A>G	NP_001447.2:p.Thr1978Ala