Canonical Allele Identifier: CA415196602
Gene: FLNA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154353186T>C , CM000685.2:g.154353186T>C GRCh38
NC_000023.10:g.153581554T>C , CM000685.1:g.153581554T>C GRCh37
NC_000023.9:g.153234748T>C NCBI36
NG_011506.1:g.26453A>G
NG_011506.2:g.26453A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.6017A>G ENSP00000353467.4:p.Lys2006Arg
ENST00000369850.10:c.6041A>G MANE Select ENSP00000358866.3:p.Lys2014Arg
ENST00000369856.8:c.5960A>G ENSP00000358872.4:p.Lys1987Arg
ENST00000422373.6:c.3161-511A>G ENSP00000416926.2:n.3161-511A>G
ENST00000610817.5:c.6098A>G ENSP00000480593.2:n.6098A>G
ENST00000673639.2:c.280-4496A>G
ENST00000676696.1:c.6320A>G ENSP00000503392.1:n.6320A>G
ENST00000678304.1:n.1220A>G
ENST00000344736.8:c.5921A>G ENSP00000358863.3:p.Lys1974Arg
ENST00000360319.8:c.6017A>G ENSP00000353467.4:p.Lys2006Arg
ENST00000369850.7:c.6041A>G ENSP00000358866.3:p.Lys2014Arg
ENST00000369856.7:c.5960A>G ENSP00000358872.4:p.Lys1987Arg
ENST00000415241.1:c.243A>G
ENST00000420627.5:c.5997A>G ENSP00000408921.1:n.5997A>G
ENST00000422373.5:c.6017A>G ENSP00000416926.1:p.Lys2006Arg
ENST00000466325.1:n.180A>G
ENST00000490936.5:n.2030A>G
ENST00000610817.4:c.5844+207A>G ENSP00000480593.1:n.5844+207A>G
NM_001110556.1:c.6041A>G NP_001104026.1:p.Lys2014Arg
NM_001456.3:c.6017A>G NP_001447.2:p.Lys2006Arg
XM_011531127.1:c.5945A>G XP_011529429.1:p.Lys1982Arg
XM_011531128.1:c.5921A>G XP_011529430.1:p.Lys1974Arg
XM_011531129.1:c.5867A>G XP_011529431.1:p.Lys1956Arg
XM_011531130.1:c.5843A>G XP_011529432.1:p.Lys1948Arg
XM_011531131.1:c.5840A>G XP_011529433.1:p.Lys1947Arg
NM_001110556.2:c.6041A>G MANE Select NP_001104026.1:p.Lys2014Arg
NM_001456.4:c.6017A>G NP_001447.2:p.Lys2006Arg