Canonical Allele Identifier: CA415197132
Gene: FLNA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154353320T>C , CM000685.2:g.154353320T>C GRCh38
NC_000023.10:g.153581688T>C , CM000685.1:g.153581688T>C GRCh37
NC_000023.9:g.153234882T>C NCBI36
NG_011506.1:g.26319A>G
NG_011506.2:g.26319A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.5974A>G ENSP00000353467.4:p.Lys1992Glu
ENST00000369850.10:c.5998A>G MANE Select ENSP00000358866.3:p.Lys2000Glu
ENST00000369856.8:c.5917A>G ENSP00000358872.4:p.Lys1973Glu
ENST00000422373.6:c.3161-645A>G ENSP00000416926.2:n.3161-645A>G
ENST00000610817.5:c.6055A>G ENSP00000480593.2:n.6055A>G
ENST00000673639.2:c.280-4630A>G
ENST00000676696.1:c.6277A>G ENSP00000503392.1:n.6277A>G
ENST00000678304.1:n.1177A>G
ENST00000344736.8:c.5878A>G ENSP00000358863.3:p.Lys1960Glu
ENST00000360319.8:c.5974A>G ENSP00000353467.4:p.Lys1992Glu
ENST00000369850.7:c.5998A>G ENSP00000358866.3:p.Lys2000Glu
ENST00000369856.7:c.5917A>G ENSP00000358872.4:p.Lys1973Glu
ENST00000415241.1:c.183A>G
ENST00000420627.5:c.5954A>G ENSP00000408921.1:n.5954A>G
ENST00000422373.5:c.5974A>G ENSP00000416926.1:p.Lys1992Glu
ENST00000438732.2:c.672A>G
ENST00000466325.1:n.137A>G
ENST00000490936.5:n.1987A>G
ENST00000610817.4:c.5844+73A>G ENSP00000480593.1:n.5844+73A>G
NM_001110556.1:c.5998A>G NP_001104026.1:p.Lys2000Glu
NM_001456.3:c.5974A>G NP_001447.2:p.Lys1992Glu
XM_011531127.1:c.5902A>G XP_011529429.1:p.Lys1968Glu
XM_011531128.1:c.5878A>G XP_011529430.1:p.Lys1960Glu
XM_011531129.1:c.5824A>G XP_011529431.1:p.Lys1942Glu
XM_011531130.1:c.5800A>G XP_011529432.1:p.Lys1934Glu
XM_011531131.1:c.5797A>G XP_011529433.1:p.Lys1933Glu
NM_001110556.2:c.5998A>G MANE Select NP_001104026.1:p.Lys2000Glu
NM_001456.4:c.5974A>G NP_001447.2:p.Lys1992Glu