Canonical Allele Identifier: CA2466653072
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154352801T= , CM000685.2:g.154352801T= GRCh38
NC_000023.10:g.153581169T= , CM000685.1:g.153581169T= GRCh37
NC_000023.9:g.153234363T= NCBI36
NG_011506.1:g.26838A=
NG_011506.2:g.26838A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.6326A= ENSP00000353467.4:p.Asn2109=
ENST00000369850.10:c.6350A= MANE Select ENSP00000358866.3:p.Asn2117=
ENST00000369856.8:c.6269A= ENSP00000358872.4:p.Asn2090=
ENST00000422373.6:c.3161-126A= ENSP00000416926.2:n.3161-126A=
ENST00000610817.5:c.6407A= ENSP00000480593.2:n.6407A=
ENST00000673639.2:c.280-4111A=
ENST00000676696.1:c.6629A= ENSP00000503392.1:n.6629A=
ENST00000678304.1:n.1529A=
ENST00000344736.8:c.6230A= ENSP00000358863.3:p.Asn2077=
ENST00000360319.8:c.6326A= ENSP00000353467.4:p.Asn2109=
ENST00000369850.7:c.6350A= ENSP00000358866.3:p.Asn2117=
ENST00000369856.7:c.6269A= ENSP00000358872.4:p.Asn2090=
ENST00000415241.1:c.552A=
ENST00000420627.5:c.6306A= ENSP00000408921.1:n.6306A=
ENST00000422373.5:c.6326A= ENSP00000416926.1:p.Asn2109=
ENST00000444578.1:c.293A= ENSP00000397824.1:p.Asn98=
ENST00000466325.1:n.565A=
ENST00000490936.5:n.2339A=
ENST00000498411.1:n.67+16A=
ENST00000610817.4:c.5844+592A= ENSP00000480593.1:n.5844+592A=
NM_001110556.1:c.6350A= NP_001104026.1:p.Asn2117=
NM_001456.3:c.6326A= NP_001447.2:p.Asn2109=
XM_011531127.1:c.6254A= XP_011529429.1:p.Asn2085=
XM_011531128.1:c.6230A= XP_011529430.1:p.Asn2077=
XM_011531129.1:c.6176A= XP_011529431.1:p.Asn2059=
XM_011531130.1:c.6152A= XP_011529432.1:p.Asn2051=
XM_011531131.1:c.6149A= XP_011529433.1:p.Asn2050=
NM_001110556.2:c.6350A= MANE Select NP_001104026.1:p.Asn2117=
NM_001456.4:c.6326A= NP_001447.2:p.Asn2109=