Canonical Allele Identifier: CA2695237783
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154353025del , CM000685.2:g.154353025del GRCh38
NC_000023.10:g.153581393del , CM000685.1:g.153581393del GRCh37
NC_000023.9:g.153234587del NCBI36
NG_011506.1:g.26616del
NG_011506.2:g.26616del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.6180del ENSP00000353467.4:p.Phe2060LeufsTer?
ENST00000369850.10:c.6204del MANE Select ENSP00000358866.3:p.Phe2068LeufsTer?
ENST00000369856.8:c.6123del ENSP00000358872.4:p.Phe2041LeufsTer?
ENST00000422373.6:c.3161-348del ENSP00000416926.2:n.3161-348del
ENST00000610817.5:c.6261del ENSP00000480593.2:n.6261del
ENST00000673639.2:c.280-4333del
ENST00000676696.1:c.6483del ENSP00000503392.1:n.6483del
ENST00000678304.1:n.1383del
ENST00000344736.8:c.6084del ENSP00000358863.3:p.Phe2028LeufsTer?
ENST00000360319.8:c.6180del ENSP00000353467.4:p.Phe2060LeufsTer?
ENST00000369850.7:c.6204del ENSP00000358866.3:p.Phe2068LeufsTer?
ENST00000369856.7:c.6123del ENSP00000358872.4:p.Phe2041LeufsTer?
ENST00000415241.1:c.406del
ENST00000420627.5:c.6160del ENSP00000408921.1:n.6160del
ENST00000422373.5:c.6180del ENSP00000416926.1:p.Phe2060LeufsTer?
ENST00000444578.1:c.147del ENSP00000397824.1:p.Phe49LeufsTer?
ENST00000466325.1:n.343del
ENST00000490936.5:n.2193del
ENST00000610817.4:c.5844+370del ENSP00000480593.1:n.5844+370del
NM_001110556.1:c.6204del NP_001104026.1:p.Phe2068LeufsTer?
NM_001456.3:c.6180del NP_001447.2:p.Phe2060LeufsTer?
XM_011531127.1:c.6108del XP_011529429.1:p.Phe2036LeufsTer?
XM_011531128.1:c.6084del XP_011529430.1:p.Phe2028LeufsTer?
XM_011531129.1:c.6030del XP_011529431.1:p.Phe2010LeufsTer?
XM_011531130.1:c.6006del XP_011529432.1:p.Phe2002LeufsTer?
XM_011531131.1:c.6003del XP_011529433.1:p.Phe2001LeufsTer?
NM_001110556.2:c.6204del MANE Select NP_001104026.1:p.Phe2068LeufsTer?
NM_001456.4:c.6180del NP_001447.2:p.Phe2060LeufsTer?