Canonical Allele Identifier: CA2466653064
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154352780T= , CM000685.2:g.154352780T= GRCh38
NC_000023.10:g.153581148T= , CM000685.1:g.153581148T= GRCh37
NC_000023.9:g.153234342T= NCBI36
NG_011506.1:g.26859A=
NG_011506.2:g.26859A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.6347A= ENSP00000353467.4:p.His2116=
ENST00000369850.10:c.6371A= MANE Select ENSP00000358866.3:p.His2124=
ENST00000369856.8:c.6290A= ENSP00000358872.4:p.His2097=
ENST00000422373.6:c.3161-105A= ENSP00000416926.2:n.3161-105A=
ENST00000610817.5:c.6428A= ENSP00000480593.2:n.6428A=
ENST00000673639.2:c.280-4090A=
ENST00000676696.1:c.6650A= ENSP00000503392.1:n.6650A=
ENST00000678304.1:n.1550A=
ENST00000344736.8:c.6251A= ENSP00000358863.3:p.His2084=
ENST00000360319.8:c.6347A= ENSP00000353467.4:p.His2116=
ENST00000369850.7:c.6371A= ENSP00000358866.3:p.His2124=
ENST00000369856.7:c.6290A= ENSP00000358872.4:p.His2097=
ENST00000415241.1:c.573A=
ENST00000420627.5:c.6327A= ENSP00000408921.1:n.6327A=
ENST00000422373.5:c.6347A= ENSP00000416926.1:p.His2116=
ENST00000444578.1:c.314A= ENSP00000397824.1:p.His105=
ENST00000466325.1:n.586A=
ENST00000474358.5:n.4A=
ENST00000490936.5:n.2360A=
ENST00000498411.1:n.67+37A=
ENST00000610817.4:c.5844+613A= ENSP00000480593.1:n.5844+613A=
NM_001110556.1:c.6371A= NP_001104026.1:p.His2124=
NM_001456.3:c.6347A= NP_001447.2:p.His2116=
XM_011531127.1:c.6275A= XP_011529429.1:p.His2092=
XM_011531128.1:c.6251A= XP_011529430.1:p.His2084=
XM_011531129.1:c.6197A= XP_011529431.1:p.His2066=
XM_011531130.1:c.6173A= XP_011529432.1:p.His2058=
XM_011531131.1:c.6170A= XP_011529433.1:p.His2057=
NM_001110556.2:c.6371A= MANE Select NP_001104026.1:p.His2124=
NM_001456.4:c.6347A= NP_001447.2:p.His2116=