Canonical Allele Identifier: CA2466653116
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154352913G= , CM000685.2:g.154352913G= GRCh38
NC_000023.10:g.153581281G= , CM000685.1:g.153581281G= GRCh37
NC_000023.9:g.153234475G= NCBI36
NG_011506.1:g.26726C=
NG_011506.2:g.26726C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360319.9:c.6214C= ENSP00000353467.4:p.Leu2072=
ENST00000369850.10:c.6238C= MANE Select ENSP00000358866.3:p.Leu2080=
ENST00000369856.8:c.6157C= ENSP00000358872.4:p.Leu2053=
ENST00000422373.6:c.3161-238C= ENSP00000416926.2:n.3161-238C=
ENST00000610817.5:c.6295C= ENSP00000480593.2:n.6295C=
ENST00000673639.2:c.280-4223C=
ENST00000676696.1:c.6517C= ENSP00000503392.1:n.6517C=
ENST00000678304.1:n.1417C=
ENST00000344736.8:c.6118C= ENSP00000358863.3:p.Leu2040=
ENST00000360319.8:c.6214C= ENSP00000353467.4:p.Leu2072=
ENST00000369850.7:c.6238C= ENSP00000358866.3:p.Leu2080=
ENST00000369856.7:c.6157C= ENSP00000358872.4:p.Leu2053=
ENST00000415241.1:c.440C=
ENST00000420627.5:c.6194C= ENSP00000408921.1:n.6194C=
ENST00000422373.5:c.6214C= ENSP00000416926.1:p.Leu2072=
ENST00000444578.1:c.181C= ENSP00000397824.1:p.Leu61=
ENST00000466325.1:n.453C=
ENST00000490936.5:n.2227C=
ENST00000610817.4:c.5844+480C= ENSP00000480593.1:n.5844+480C=
NM_001110556.1:c.6238C= NP_001104026.1:p.Leu2080=
NM_001456.3:c.6214C= NP_001447.2:p.Leu2072=
XM_011531127.1:c.6142C= XP_011529429.1:p.Leu2048=
XM_011531128.1:c.6118C= XP_011529430.1:p.Leu2040=
XM_011531129.1:c.6064C= XP_011529431.1:p.Leu2022=
XM_011531130.1:c.6040C= XP_011529432.1:p.Leu2014=
XM_011531131.1:c.6037C= XP_011529433.1:p.Leu2013=
NM_001110556.2:c.6238C= MANE Select NP_001104026.1:p.Leu2080=
NM_001456.4:c.6214C= NP_001447.2:p.Leu2072=