Canonical Allele Identifier: CA2466655509
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154359138G= , CM000685.2:g.154359138G= GRCh38
NC_000023.10:g.153587506G= , CM000685.1:g.153587506G= GRCh37
NC_000023.9:g.153240700G= NCBI36
NG_011506.1:g.20501C=
NG_011506.2:g.20501C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.4320C= ENSP00000353467.4:p.Val1440=
ENST00000369850.10:c.4320C= MANE Select ENSP00000358866.3:p.Val1440=
ENST00000369856.8:c.4239C= ENSP00000358872.4:p.Val1413=
ENST00000422373.6:c.3160+2217C= ENSP00000416926.2:n.3160+2217C=
ENST00000610817.5:c.4377C= ENSP00000480593.2:n.4377C=
ENST00000673639.2:c.279+6298C=
ENST00000676696.1:c.4599C= ENSP00000503392.1:n.4599C=
ENST00000678304.1:n.99C=
ENST00000344736.8:c.4320C= ENSP00000358863.3:p.Val1440=
ENST00000360319.8:c.4320C= ENSP00000353467.4:p.Val1440=
ENST00000369850.7:c.4320C= ENSP00000358866.3:p.Val1440=
ENST00000369856.7:c.4239C= ENSP00000358872.4:p.Val1413=
ENST00000420627.5:c.4276C= ENSP00000408921.1:n.4276C=
ENST00000422373.5:c.4320C= ENSP00000416926.1:p.Val1440=
ENST00000490936.5:n.333C=
ENST00000610817.4:c.4239C= ENSP00000480593.1:p.Val1413=
NM_001110556.1:c.4320C= NP_001104026.1:p.Val1440=
NM_001456.3:c.4320C= NP_001447.2:p.Val1440=
XM_011531127.1:c.4320C= XP_011529429.1:p.Val1440=
XM_011531128.1:c.4320C= XP_011529430.1:p.Val1440=
XM_011531129.1:c.4320C= XP_011529431.1:p.Val1440=
XM_011531130.1:c.4320C= XP_011529432.1:p.Val1440=
XM_011531131.1:c.4119C= XP_011529433.1:p.Val1373=
NM_001110556.2:c.4320C= MANE Select NP_001104026.1:p.Val1440=
NM_001456.4:c.4320C= NP_001447.2:p.Val1440=