Canonical Allele Identifier: CA2824282224
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154352677_154352772del , CM000685.2:g.154352677_154352772del GRCh38
NC_000023.10:g.153581045_153581140del , CM000685.1:g.153581045_153581140del GRCh37
NC_000023.9:g.153234239_153234334del NCBI36
NG_011506.1:g.26869_26964del
NG_011506.2:g.26869_26964del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.6355+2_6356del
ENST00000369850.10:c.6379+2_6380del
ENST00000369856.8:c.6298+2_6299del
ENST00000422373.6:c.3161-95_3161del
ENST00000610817.5:c.6436+2_6437del
ENST00000673639.2:c.280-4080_280-3985del
ENST00000676696.1:c.6658+2_6659del
ENST00000678304.1:n.1558+2_1559del
ENST00000344736.8:c.6259+2_6260del
ENST00000360319.8:c.6355+2_6356del
ENST00000369850.7:c.6379+2_6380del
ENST00000369856.7:c.6298+2_6299del
ENST00000415241.1:c.581+2_582del
ENST00000420627.5:c.6335+2_6336del
ENST00000422373.5:c.6355+2_6356del
ENST00000444578.1:c.322+2_322+97del
ENST00000466325.1:n.596_691del
ENST00000474358.5:n.12+2_13del
ENST00000490936.5:n.2368+2_2369del
ENST00000498411.1:n.67+47_67+142del
ENST00000610817.4:c.5844+623_5844+718del ENSP00000480593.1:n.5844+623_5844+718del
NM_001110556.1:c.6379+2_6380del
NM_001456.3:c.6355+2_6356del
XM_011531127.1:c.6283+2_6284del
XM_011531128.1:c.6259+2_6260del
XM_011531129.1:c.6205+2_6206del
XM_011531130.1:c.6181+2_6182del
XM_011531131.1:c.6178+2_6179del
NM_001110556.2:c.6379+2_6380del
NM_001456.4:c.6355+2_6356del