Canonical Allele Identifier: CA2695112896
Gene: FLNA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154358765_154358768del , CM000685.2:g.154358765_154358768del GRCh38
NC_000023.10:g.153587133_153587136del , CM000685.1:g.153587133_153587136del GRCh37
NC_000023.9:g.153240327_153240330del NCBI36
NG_011506.1:g.20880_20883del
NG_011506.2:g.20880_20883del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.4475-191_4475-188del ENSP00000353467.4:n.4475-191_4475-188del
ENST00000369850.10:c.4475-191_4475-188del MANE Select ENSP00000358866.3:n.4475-191_4475-188del
ENST00000369856.8:c.4394-191_4394-188del ENSP00000358872.4:n.4394-191_4394-188del
ENST00000422373.6:c.3160+2596_3160+2599del ENSP00000416926.2:n.3160+2596_3160+2599del
ENST00000610817.5:c.4532-191_4532-188del ENSP00000480593.2:n.4532-191_4532-188del
ENST00000673639.2:c.279+6677_279+6680del
ENST00000676696.1:c.4754-191_4754-188del ENSP00000503392.1:n.4754-191_4754-188del
ENST00000678304.1:n.148+330_148+333del
ENST00000344736.8:c.4475-191_4475-188del ENSP00000358863.3:n.4475-191_4475-188del
ENST00000360319.8:c.4475-191_4475-188del ENSP00000353467.4:n.4475-191_4475-188del
ENST00000369850.7:c.4475-191_4475-188del ENSP00000358866.3:n.4475-191_4475-188del
ENST00000369856.7:c.4394-191_4394-188del ENSP00000358872.4:n.4394-191_4394-188del
ENST00000420627.5:c.4431-191_4431-188del ENSP00000408921.1:n.4431-191_4431-188del
ENST00000422373.5:c.4475-191_4475-188del ENSP00000416926.1:n.4475-191_4475-188del
ENST00000490936.5:n.488-191_488-188del
ENST00000610817.4:c.4394-191_4394-188del ENSP00000480593.1:n.4394-191_4394-188del
NM_001110556.1:c.4475-191_4475-188del NP_001104026.1:n.4475-191_4475-188del
NM_001456.3:c.4475-191_4475-188del NP_001447.2:n.4475-191_4475-188del
XM_011531127.1:c.4475-191_4475-188del XP_011529429.1:n.4475-191_4475-188del
XM_011531128.1:c.4475-191_4475-188del XP_011529430.1:n.4475-191_4475-188del
XM_011531129.1:c.4475-191_4475-188del XP_011529431.1:n.4475-191_4475-188del
XM_011531130.1:c.4475-191_4475-188del XP_011529432.1:n.4475-191_4475-188del
XM_011531131.1:c.4274-191_4274-188del XP_011529433.1:n.4274-191_4274-188del
NM_001110556.2:c.4475-191_4475-188del MANE Select NP_001104026.1:n.4475-191_4475-188del
NM_001456.4:c.4475-191_4475-188del NP_001447.2:n.4475-191_4475-188del