Canonical Allele Identifier: CA2579738021
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154359098_154359099del , CM000685.2:g.154359098_154359099del GRCh38
NC_000023.10:g.153587466_153587467del , CM000685.1:g.153587466_153587467del GRCh37
NC_000023.9:g.153240660_153240661del NCBI36
NG_011506.1:g.20542_20543del
NG_011506.2:g.20542_20543del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.4361_4362del ENSP00000353467.4:p.Ser1454TrpfsTer?
ENST00000369850.10:c.4361_4362del MANE Select ENSP00000358866.3:p.Ser1454TrpfsTer?
ENST00000369856.8:c.4280_4281del ENSP00000358872.4:p.Ser1427TrpfsTer?
ENST00000422373.6:c.3160+2258_3160+2259del ENSP00000416926.2:n.3160+2258_3160+2259del
ENST00000610817.5:c.4418_4419del ENSP00000480593.2:n.4418_4419del
ENST00000673639.2:c.279+6339_279+6340del
ENST00000676696.1:c.4640_4641del ENSP00000503392.1:n.4640_4641del
ENST00000678304.1:n.140_141del
ENST00000344736.8:c.4361_4362del ENSP00000358863.3:p.Ser1454TrpfsTer?
ENST00000360319.8:c.4361_4362del ENSP00000353467.4:p.Ser1454TrpfsTer?
ENST00000369850.7:c.4361_4362del ENSP00000358866.3:p.Ser1454TrpfsTer?
ENST00000369856.7:c.4280_4281del ENSP00000358872.4:p.Ser1427TrpfsTer?
ENST00000420627.5:c.4317_4318del ENSP00000408921.1:n.4317_4318del
ENST00000422373.5:c.4361_4362del ENSP00000416926.1:p.Ser1454TrpfsTer?
ENST00000490936.5:n.374_375del
ENST00000610817.4:c.4280_4281del ENSP00000480593.1:p.Ser1427TrpfsTer?
NM_001110556.1:c.4361_4362del NP_001104026.1:p.Ser1454TrpfsTer?
NM_001456.3:c.4361_4362del NP_001447.2:p.Ser1454TrpfsTer?
XM_011531127.1:c.4361_4362del XP_011529429.1:p.Ser1454TrpfsTer?
XM_011531128.1:c.4361_4362del XP_011529430.1:p.Ser1454TrpfsTer?
XM_011531129.1:c.4361_4362del XP_011529431.1:p.Ser1454TrpfsTer?
XM_011531130.1:c.4361_4362del XP_011529432.1:p.Ser1454TrpfsTer?
XM_011531131.1:c.4160_4161del XP_011529433.1:p.Ser1387TrpfsTer?
NM_001110556.2:c.4361_4362del MANE Select NP_001104026.1:p.Ser1454TrpfsTer?
NM_001456.4:c.4361_4362del NP_001447.2:p.Ser1454TrpfsTer?