Canonical Allele Identifier: CA415191955

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352576C>T , CM000685.2:g.154352576C>T	GRCh38
NC_000023.10:g.153580944C>T , CM000685.1:g.153580944C>T	GRCh37
NC_000023.9:g.153234138C>T	NCBI36
NG_011506.1:g.27063G>A
NG_011506.2:g.27063G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001110556.2:c.6479G>A MANE Select	NP_001104026.1:p.Cys2160Tyr
ENST00000369850.10:c.6479G>A MANE Select	ENSP00000358866.3:p.Cys2160Tyr
NM_001110556.1:c.6479G>A	NP_001104026.1:p.Cys2160Tyr
NM_001456.3:c.6455G>A	NP_001447.2:p.Cys2152Tyr
NM_001456.4:c.6455G>A	NP_001447.2:p.Cys2152Tyr
ENST00000344736.8:c.6359G>A	ENSP00000358863.3:p.Cys2120Tyr
ENST00000360319.8:c.6455G>A	ENSP00000353467.4:p.Cys2152Tyr
ENST00000360319.9:c.6455G>A	ENSP00000353467.4:p.Cys2152Tyr
ENST00000369850.7:c.6479G>A	ENSP00000358866.3:p.Cys2160Tyr
ENST00000369856.7:c.6398G>A	ENSP00000358872.4:p.Cys2133Tyr
ENST00000369856.8:c.6398G>A	ENSP00000358872.4:p.Cys2133Tyr
ENST00000415241.1:c.681G>A
ENST00000420627.5:c.6435G>A	ENSP00000408921.1:n.6435G>A
ENST00000422373.5:c.6455G>A	ENSP00000416926.1:p.Cys2152Tyr
ENST00000422373.6:c.3260G>A	ENSP00000416926.2:p.Cys1087Tyr
ENST00000444578.1:c.323-129G>A	ENSP00000397824.1:n.323-129G>A
ENST00000466325.1:n.790G>A
ENST00000474358.5:n.112G>A
ENST00000490936.5:n.2468G>A
ENST00000498411.1:n.67+241G>A
ENST00000610817.4:c.5845-626G>A	ENSP00000480593.1:n.5845-626G>A
ENST00000610817.5:c.6536G>A	ENSP00000480593.2:n.6536G>A
ENST00000673639.2:c.280-3886G>A
ENST00000676696.1:c.6758G>A	ENSP00000503392.1:n.6758G>A
ENST00000678304.1:n.1658G>A
XM_011531127.1:c.6383G>A	XP_011529429.1:p.Cys2128Tyr
XM_011531128.1:c.6359G>A	XP_011529430.1:p.Cys2120Tyr
XM_011531129.1:c.6305G>A	XP_011529431.1:p.Cys2102Tyr
XM_011531130.1:c.6281G>A	XP_011529432.1:p.Cys2094Tyr
XM_011531131.1:c.6278G>A	XP_011529433.1:p.Cys2093Tyr