Canonical Allele Identifier: CA645290407
Gene: FLNA HGNC NCBI

Linked Data

dbSNP Id: rs1569551859

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154367613_154367614dup , CM000685.2:g.154367613_154367614dup GRCh38
NC_000023.10:g.153595981_153595982dup , CM000685.1:g.153595981_153595982dup GRCh37
NC_000023.9:g.153249175_153249176dup NCBI36
NG_011506.1:g.12026_12027dup
NG_011506.2:g.12026_12027dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.720+28_720+29dup ENSP00000353467.4:n.720+28_720+29dup
ENST00000369850.10:c.720+28_720+29dup MANE Select ENSP00000358866.3:n.720+28_720+29dup
ENST00000369856.8:c.639+28_639+29dup ENSP00000358872.4:n.639+28_639+29dup
ENST00000422373.6:c.720+28_720+29dup ENSP00000416926.2:n.720+28_720+29dup
ENST00000610817.5:c.720+28_720+29dup ENSP00000480593.2:n.720+28_720+29dup
ENST00000676696.1:c.720+28_720+29dup ENSP00000503392.1:n.720+28_720+29dup
ENST00000344736.8:c.720+28_720+29dup ENSP00000358863.3:n.720+28_720+29dup
ENST00000360319.8:c.720+28_720+29dup ENSP00000353467.4:n.720+28_720+29dup
ENST00000369850.7:c.720+28_720+29dup ENSP00000358866.3:n.720+28_720+29dup
ENST00000369856.7:c.639+28_639+29dup ENSP00000358872.4:n.639+28_639+29dup
ENST00000420627.5:c.678+28_678+29dup ENSP00000408921.1:n.678+28_678+29dup
ENST00000422373.5:c.720+28_720+29dup ENSP00000416926.1:n.720+28_720+29dup
ENST00000610817.4:c.639+28_639+29dup ENSP00000480593.1:n.639+28_639+29dup
NM_001110556.1:c.720+28_720+29dup NP_001104026.1:n.720+28_720+29dup
NM_001456.3:c.720+28_720+29dup NP_001447.2:n.720+28_720+29dup
XM_011531127.1:c.720+28_720+29dup XP_011529429.1:n.720+28_720+29dup
XM_011531128.1:c.720+28_720+29dup XP_011529430.1:n.720+28_720+29dup
XM_011531129.1:c.720+28_720+29dup XP_011529431.1:n.720+28_720+29dup
XM_011531130.1:c.720+28_720+29dup XP_011529432.1:n.720+28_720+29dup
XM_011531131.1:c.720+28_720+29dup XP_011529433.1:n.720+28_720+29dup
NM_001110556.2:c.720+28_720+29dup MANE Select NP_001104026.1:n.720+28_720+29dup
NM_001456.4:c.720+28_720+29dup NP_001447.2:n.720+28_720+29dup