Canonical Allele Identifier: CA2695111957
Gene: FLNA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154352811_154352813del , CM000685.2:g.154352811_154352813del GRCh38
NC_000023.10:g.153581179_153581181del , CM000685.1:g.153581179_153581181del GRCh37
NC_000023.9:g.153234373_153234375del NCBI36
NG_011506.1:g.26828_26830del
NG_011506.2:g.26828_26830del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.6316_6318del ENSP00000353467.4:p.Tyr2106del
ENST00000369850.10:c.6340_6342del MANE Select ENSP00000358866.3:p.Tyr2114del
ENST00000369856.8:c.6259_6261del ENSP00000358872.4:p.Tyr2087del
ENST00000422373.6:c.3161-136_3161-134del ENSP00000416926.2:n.3161-136_3161-134del
ENST00000610817.5:c.6397_6399del ENSP00000480593.2:n.6397_6399del
ENST00000673639.2:c.280-4121_280-4119del
ENST00000676696.1:c.6619_6621del ENSP00000503392.1:n.6619_6621del
ENST00000678304.1:n.1519_1521del
ENST00000344736.8:c.6220_6222del ENSP00000358863.3:p.Tyr2074del
ENST00000360319.8:c.6316_6318del ENSP00000353467.4:p.Tyr2106del
ENST00000369850.7:c.6340_6342del ENSP00000358866.3:p.Tyr2114del
ENST00000369856.7:c.6259_6261del ENSP00000358872.4:p.Tyr2087del
ENST00000415241.1:c.542_544del
ENST00000420627.5:c.6296_6298del ENSP00000408921.1:n.6296_6298del
ENST00000422373.5:c.6316_6318del ENSP00000416926.1:p.Tyr2106del
ENST00000444578.1:c.283_285del ENSP00000397824.1:p.Tyr95del
ENST00000466325.1:n.555_557del
ENST00000490936.5:n.2329_2331del
ENST00000498411.1:n.67+6_67+8del
ENST00000610817.4:c.5844+582_5844+584del ENSP00000480593.1:n.5844+582_5844+584del
NM_001110556.1:c.6340_6342del NP_001104026.1:p.Tyr2114del
NM_001456.3:c.6316_6318del NP_001447.2:p.Tyr2106del
XM_011531127.1:c.6244_6246del XP_011529429.1:p.Tyr2082del
XM_011531128.1:c.6220_6222del XP_011529430.1:p.Tyr2074del
XM_011531129.1:c.6166_6168del XP_011529431.1:p.Tyr2056del
XM_011531130.1:c.6142_6144del XP_011529432.1:p.Tyr2048del
XM_011531131.1:c.6139_6141del XP_011529433.1:p.Tyr2047del
NM_001110556.2:c.6340_6342del MANE Select NP_001104026.1:p.Tyr2114del
NM_001456.4:c.6316_6318del NP_001447.2:p.Tyr2106del