Canonical Allele Identifier: CA2506895596
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154352933_154352934del , CM000685.2:g.154352933_154352934del GRCh38
NC_000023.10:g.153581301_153581302del , CM000685.1:g.153581301_153581302del GRCh37
NC_000023.9:g.153234495_153234496del NCBI36
NG_011506.1:g.26705_26706del
NG_011506.2:g.26705_26706del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.6203-10_6203-9del ENSP00000353467.4:n.6203-10_6203-9del
ENST00000369850.10:c.6227-10_6227-9del MANE Select ENSP00000358866.3:n.6227-10_6227-9del
ENST00000369856.8:c.6146-10_6146-9del ENSP00000358872.4:n.6146-10_6146-9del
ENST00000422373.6:c.3161-259_3161-258del ENSP00000416926.2:n.3161-259_3161-258del
ENST00000610817.5:c.6284-10_6284-9del ENSP00000480593.2:n.6284-10_6284-9del
ENST00000673639.2:c.280-4244_280-4243del
ENST00000676696.1:c.6506-10_6506-9del ENSP00000503392.1:n.6506-10_6506-9del
ENST00000678304.1:n.1406-10_1406-9del
ENST00000344736.8:c.6107-10_6107-9del ENSP00000358863.3:n.6107-10_6107-9del
ENST00000360319.8:c.6203-10_6203-9del ENSP00000353467.4:n.6203-10_6203-9del
ENST00000369850.7:c.6227-10_6227-9del ENSP00000358866.3:n.6227-10_6227-9del
ENST00000369856.7:c.6146-10_6146-9del ENSP00000358872.4:n.6146-10_6146-9del
ENST00000415241.1:c.429-10_429-9del
ENST00000420627.5:c.6183-10_6183-9del ENSP00000408921.1:n.6183-10_6183-9del
ENST00000422373.5:c.6203-10_6203-9del ENSP00000416926.1:n.6203-10_6203-9del
ENST00000444578.1:c.170-10_170-9del ENSP00000397824.1:n.170-10_170-9del
ENST00000466325.1:n.432_433del
ENST00000490936.5:n.2216-10_2216-9del
ENST00000610817.4:c.5844+459_5844+460del ENSP00000480593.1:n.5844+459_5844+460del
NM_001110556.1:c.6227-10_6227-9del NP_001104026.1:n.6227-10_6227-9del
NM_001456.3:c.6203-10_6203-9del NP_001447.2:n.6203-10_6203-9del
XM_011531127.1:c.6131-10_6131-9del XP_011529429.1:n.6131-10_6131-9del
XM_011531128.1:c.6107-10_6107-9del XP_011529430.1:n.6107-10_6107-9del
XM_011531129.1:c.6053-10_6053-9del XP_011529431.1:n.6053-10_6053-9del
XM_011531130.1:c.6029-10_6029-9del XP_011529432.1:n.6029-10_6029-9del
XM_011531131.1:c.6026-10_6026-9del XP_011529433.1:n.6026-10_6026-9del
NM_001110556.2:c.6227-10_6227-9del MANE Select NP_001104026.1:n.6227-10_6227-9del
NM_001456.4:c.6203-10_6203-9del NP_001447.2:n.6203-10_6203-9del