Canonical Allele Identifier: CA415193540

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581194T>C (hg19) ; chrX:g.154352826T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352826T>C , CM000685.2:g.154352826T>C	GRCh38
NC_000023.10:g.153581194T>C , CM000685.1:g.153581194T>C	GRCh37
NC_000023.9:g.153234388T>C	NCBI36
NG_011506.1:g.26813A>G
NG_011506.2:g.26813A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6301A>G	ENSP00000353467.4:p.Thr2101Ala
ENST00000369850.10:c.6325A>G MANE Select	ENSP00000358866.3:p.Thr2109Ala
ENST00000369856.8:c.6244A>G	ENSP00000358872.4:p.Thr2082Ala
ENST00000422373.6:c.3161-151A>G	ENSP00000416926.2:n.3161-151A>G
ENST00000610817.5:c.6382A>G	ENSP00000480593.2:n.6382A>G
ENST00000673639.2:c.280-4136A>G
ENST00000676696.1:c.6604A>G	ENSP00000503392.1:n.6604A>G
ENST00000678304.1:n.1504A>G
ENST00000344736.8:c.6205A>G	ENSP00000358863.3:p.Thr2069Ala
ENST00000360319.8:c.6301A>G	ENSP00000353467.4:p.Thr2101Ala
ENST00000369850.7:c.6325A>G	ENSP00000358866.3:p.Thr2109Ala
ENST00000369856.7:c.6244A>G	ENSP00000358872.4:p.Thr2082Ala
ENST00000415241.1:c.527A>G
ENST00000420627.5:c.6281A>G	ENSP00000408921.1:n.6281A>G
ENST00000422373.5:c.6301A>G	ENSP00000416926.1:p.Thr2101Ala
ENST00000444578.1:c.268A>G	ENSP00000397824.1:p.Thr90Ala
ENST00000466325.1:n.540A>G
ENST00000490936.5:n.2314A>G
ENST00000498411.1:n.58A>G
ENST00000610817.4:c.5844+567A>G	ENSP00000480593.1:n.5844+567A>G
NM_001110556.1:c.6325A>G	NP_001104026.1:p.Thr2109Ala
NM_001456.3:c.6301A>G	NP_001447.2:p.Thr2101Ala
XM_011531127.1:c.6229A>G	XP_011529429.1:p.Thr2077Ala
XM_011531128.1:c.6205A>G	XP_011529430.1:p.Thr2069Ala
XM_011531129.1:c.6151A>G	XP_011529431.1:p.Thr2051Ala
XM_011531130.1:c.6127A>G	XP_011529432.1:p.Thr2043Ala
XM_011531131.1:c.6124A>G	XP_011529433.1:p.Thr2042Ala
NM_001110556.2:c.6325A>G MANE Select	NP_001104026.1:p.Thr2109Ala
NM_001456.4:c.6301A>G	NP_001447.2:p.Thr2101Ala