Canonical Allele Identifier: CA2466652233
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154350557T= , CM000685.2:g.154350557T= GRCh38
NC_000023.10:g.153578925T= , CM000685.1:g.153578925T= GRCh37
NC_000023.9:g.153232119T= NCBI36
NG_011506.1:g.29082A=
NG_011506.2:g.29082A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.7133-350A= ENSP00000353467.4:n.7133-350A=
ENST00000369850.10:c.7157-350A= MANE Select ENSP00000358866.3:n.7157-350A=
ENST00000369856.8:c.7076-350A= ENSP00000358872.4:n.7076-350A=
ENST00000422373.6:c.3938-350A= ENSP00000416926.2:n.3938-350A=
ENST00000610817.5:c.7214-350A= ENSP00000480593.2:n.7214-350A=
ENST00000673639.2:c.280-1867A=
ENST00000676696.1:c.7436-350A= ENSP00000503392.1:n.7436-350A=
ENST00000678304.1:n.2875-350A=
ENST00000344736.8:c.7037-350A= ENSP00000358863.3:n.7037-350A=
ENST00000360319.8:c.7133-350A= ENSP00000353467.4:n.7133-350A=
ENST00000369850.7:c.7157-350A= ENSP00000358866.3:n.7157-350A=
ENST00000369856.7:c.7076-350A= ENSP00000358872.4:n.7076-350A=
ENST00000420627.5:c.7113-350A= ENSP00000408921.1:n.7113-350A=
ENST00000422373.5:c.7133-350A= ENSP00000416926.1:n.7133-350A=
ENST00000490936.5:n.4036A=
ENST00000498411.1:n.68-1727A=
ENST00000498491.5:n.198-350A=
ENST00000610817.4:c.6161-350A= ENSP00000480593.1:n.6161-350A=
NM_001110556.1:c.7157-350A= NP_001104026.1:n.7157-350A=
NM_001456.3:c.7133-350A= NP_001447.2:n.7133-350A=
XM_011531127.1:c.7061-350A= XP_011529429.1:n.7061-350A=
XM_011531128.1:c.7037-350A= XP_011529430.1:n.7037-350A=
XM_011531129.1:c.6983-350A= XP_011529431.1:n.6983-350A=
XM_011531130.1:c.6959-350A= XP_011529432.1:n.6959-350A=
XM_011531131.1:c.6956-350A= XP_011529433.1:n.6956-350A=
NM_001110556.2:c.7157-350A= MANE Select NP_001104026.1:n.7157-350A=
NM_001456.4:c.7133-350A= NP_001447.2:n.7133-350A=