Canonical Allele Identifier: CA415192281

Gene: FLNA

Linked Data

• dbSNP Id: rs2067628653
• MyVariant Identifiers: chrX:g.153580990T>C (hg19) ; chrX:g.154352622T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352622T>C , CM000685.2:g.154352622T>C	GRCh38
NC_000023.10:g.153580990T>C , CM000685.1:g.153580990T>C	GRCh37
NC_000023.9:g.153234184T>C	NCBI36
NG_011506.1:g.27017A>G
NG_011506.2:g.27017A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6409A>G	ENSP00000353467.4:p.Thr2137Ala
ENST00000369850.10:c.6433A>G MANE Select	ENSP00000358866.3:p.Thr2145Ala
ENST00000369856.8:c.6352A>G	ENSP00000358872.4:p.Thr2118Ala
ENST00000422373.6:c.3214A>G	ENSP00000416926.2:p.Thr1072Ala
ENST00000610817.5:c.6490A>G	ENSP00000480593.2:n.6490A>G
ENST00000673639.2:c.280-3932A>G
ENST00000676696.1:c.6712A>G	ENSP00000503392.1:n.6712A>G
ENST00000678304.1:n.1612A>G
ENST00000344736.8:c.6313A>G	ENSP00000358863.3:p.Thr2105Ala
ENST00000360319.8:c.6409A>G	ENSP00000353467.4:p.Thr2137Ala
ENST00000369850.7:c.6433A>G	ENSP00000358866.3:p.Thr2145Ala
ENST00000369856.7:c.6352A>G	ENSP00000358872.4:p.Thr2118Ala
ENST00000415241.1:c.635A>G
ENST00000420627.5:c.6389A>G	ENSP00000408921.1:n.6389A>G
ENST00000422373.5:c.6409A>G	ENSP00000416926.1:p.Thr2137Ala
ENST00000444578.1:c.322+150A>G	ENSP00000397824.1:n.322+150A>G
ENST00000466325.1:n.744A>G
ENST00000474358.5:n.66A>G
ENST00000490936.5:n.2422A>G
ENST00000498411.1:n.67+195A>G
ENST00000610817.4:c.5845-672A>G	ENSP00000480593.1:n.5845-672A>G
NM_001110556.1:c.6433A>G	NP_001104026.1:p.Thr2145Ala
NM_001456.3:c.6409A>G	NP_001447.2:p.Thr2137Ala
XM_011531127.1:c.6337A>G	XP_011529429.1:p.Thr2113Ala
XM_011531128.1:c.6313A>G	XP_011529430.1:p.Thr2105Ala
XM_011531129.1:c.6259A>G	XP_011529431.1:p.Thr2087Ala
XM_011531130.1:c.6235A>G	XP_011529432.1:p.Thr2079Ala
XM_011531131.1:c.6232A>G	XP_011529433.1:p.Thr2078Ala
NM_001110556.2:c.6433A>G MANE Select	NP_001104026.1:p.Thr2145Ala
NM_001456.4:c.6409A>G	NP_001447.2:p.Thr2137Ala