Canonical Allele Identifier: CA2824295653
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154362605dup , CM000685.2:g.154362605dup GRCh38
NC_000023.10:g.153590973dup , CM000685.1:g.153590973dup GRCh37
NC_000023.9:g.153244167dup NCBI36
NG_011506.1:g.17034dup
NG_011506.2:g.17034dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.2405-27dup ENSP00000353467.4:n.2405-27dup
ENST00000369850.10:c.2405-27dup MANE Select ENSP00000358866.3:n.2405-27dup
ENST00000369856.8:c.2324-27dup ENSP00000358872.4:n.2324-27dup
ENST00000422373.6:c.2405-27dup ENSP00000416926.2:n.2405-27dup
ENST00000610817.5:c.2462-27dup ENSP00000480593.2:n.2462-27dup
ENST00000673639.2:c.279+2831dup
ENST00000676696.1:c.2684-27dup ENSP00000503392.1:n.2684-27dup
ENST00000344736.8:c.2405-27dup ENSP00000358863.3:n.2405-27dup
ENST00000360319.8:c.2405-27dup ENSP00000353467.4:n.2405-27dup
ENST00000369850.7:c.2405-27dup ENSP00000358866.3:n.2405-27dup
ENST00000369856.7:c.2324-27dup ENSP00000358872.4:n.2324-27dup
ENST00000420627.5:c.2361-27dup ENSP00000408921.1:n.2361-27dup
ENST00000422373.5:c.2405-27dup ENSP00000416926.1:n.2405-27dup
ENST00000610817.4:c.2324-27dup ENSP00000480593.1:n.2324-27dup
NM_001110556.1:c.2405-27dup NP_001104026.1:n.2405-27dup
NM_001456.3:c.2405-27dup NP_001447.2:n.2405-27dup
XM_011531127.1:c.2405-27dup XP_011529429.1:n.2405-27dup
XM_011531128.1:c.2405-27dup XP_011529430.1:n.2405-27dup
XM_011531129.1:c.2405-27dup XP_011529431.1:n.2405-27dup
XM_011531130.1:c.2405-27dup XP_011529432.1:n.2405-27dup
XM_011531131.1:c.2204-27dup XP_011529433.1:n.2204-27dup
NM_001110556.2:c.2405-27dup MANE Select NP_001104026.1:n.2405-27dup
NM_001456.4:c.2405-27dup NP_001447.2:n.2405-27dup