Canonical Allele Identifier: CA325178

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154351640C>T , CM000685.2:g.154351640C>T	GRCh38
NC_000023.10:g.153580008C>T , CM000685.1:g.153580008C>T	GRCh37
NC_000023.9:g.153233202C>T	NCBI36
NG_011506.1:g.27999G>A
NG_011506.2:g.27999G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001110556.2:c.6964G>A MANE Select	NP_001104026.1:p.Val2322Met
ENST00000369850.10:c.6964G>A MANE Select	ENSP00000358866.3:p.Val2322Met
NM_001110556.1:c.6964G>A	NP_001104026.1:p.Val2322Met
NM_001456.3:c.6940G>A	NP_001447.2:p.Val2314Met
NM_001456.4:c.6940G>A	NP_001447.2:p.Val2314Met
ENST00000344736.8:c.6844G>A	ENSP00000358863.3:p.Val2282Met
ENST00000360319.8:c.6940G>A	ENSP00000353467.4:p.Val2314Met
ENST00000360319.9:c.6940G>A	ENSP00000353467.4:p.Val2314Met
ENST00000369850.7:c.6964G>A	ENSP00000358866.3:p.Val2322Met
ENST00000369856.7:c.6883G>A	ENSP00000358872.4:p.Val2295Met
ENST00000369856.8:c.6883G>A	ENSP00000358872.4:p.Val2295Met
ENST00000420627.5:c.6920G>A	ENSP00000408921.1:n.6920G>A
ENST00000422373.5:c.6940G>A	ENSP00000416926.1:p.Val2314Met
ENST00000422373.6:c.3745G>A	ENSP00000416926.2:p.Val1249Met
ENST00000444578.1:c.784G>A	ENSP00000397824.1:p.Val262Met
ENST00000490936.5:n.2953G>A
ENST00000498411.1:n.67+1177G>A
ENST00000610817.4:c.5968G>A	ENSP00000480593.1:p.Val1990Met
ENST00000610817.5:c.7021G>A	ENSP00000480593.2:n.7021G>A
ENST00000673639.2:c.280-2950G>A
ENST00000676696.1:c.7243G>A	ENSP00000503392.1:n.7243G>A
ENST00000678304.1:n.2143G>A
XM_011531127.1:c.6868G>A	XP_011529429.1:p.Val2290Met
XM_011531128.1:c.6844G>A	XP_011529430.1:p.Val2282Met
XM_011531129.1:c.6790G>A	XP_011529431.1:p.Val2264Met
XM_011531130.1:c.6766G>A	XP_011529432.1:p.Val2256Met
XM_011531131.1:c.6763G>A	XP_011529433.1:p.Val2255Met