Canonical Allele Identifier: CA415184742

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153579292T>C (hg19) ; chrX:g.154350924T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350924T>C , CM000685.2:g.154350924T>C	GRCh38
NC_000023.10:g.153579292T>C , CM000685.1:g.153579292T>C	GRCh37
NC_000023.9:g.153232486T>C	NCBI36
NG_011506.1:g.28715A>G
NG_011506.2:g.28715A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7117A>G	ENSP00000353467.4:p.Thr2373Ala
ENST00000369850.10:c.7141A>G MANE Select	ENSP00000358866.3:p.Thr2381Ala
ENST00000369856.8:c.7060A>G	ENSP00000358872.4:p.Thr2354Ala
ENST00000422373.6:c.3922A>G	ENSP00000416926.2:p.Thr1308Ala
ENST00000610817.5:c.7198A>G	ENSP00000480593.2:n.7198A>G
ENST00000673639.2:c.280-2234A>G
ENST00000676696.1:c.7420A>G	ENSP00000503392.1:n.7420A>G
ENST00000678304.1:n.2859A>G
ENST00000344736.8:c.7021A>G	ENSP00000358863.3:p.Thr2341Ala
ENST00000360319.8:c.7117A>G	ENSP00000353467.4:p.Thr2373Ala
ENST00000369850.7:c.7141A>G	ENSP00000358866.3:p.Thr2381Ala
ENST00000369856.7:c.7060A>G	ENSP00000358872.4:p.Thr2354Ala
ENST00000420627.5:c.7097A>G	ENSP00000408921.1:n.7097A>G
ENST00000422373.5:c.7117A>G	ENSP00000416926.1:p.Thr2373Ala
ENST00000490936.5:n.3669A>G
ENST00000498411.1:n.67+1893A>G
ENST00000498491.5:n.182A>G
ENST00000610817.4:c.6145A>G	ENSP00000480593.1:p.Thr2049Ala
NM_001110556.1:c.7141A>G	NP_001104026.1:p.Thr2381Ala
NM_001456.3:c.7117A>G	NP_001447.2:p.Thr2373Ala
XM_011531127.1:c.7045A>G	XP_011529429.1:p.Thr2349Ala
XM_011531128.1:c.7021A>G	XP_011529430.1:p.Thr2341Ala
XM_011531129.1:c.6967A>G	XP_011529431.1:p.Thr2323Ala
XM_011531130.1:c.6943A>G	XP_011529432.1:p.Thr2315Ala
XM_011531131.1:c.6940A>G	XP_011529433.1:p.Thr2314Ala
NM_001110556.2:c.7141A>G MANE Select	NP_001104026.1:p.Thr2381Ala
NM_001456.4:c.7117A>G	NP_001447.2:p.Thr2373Ala