Canonical Allele Identifier: CA2569031106
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154352970_154352971insT , CM000685.2:g.154352970_154352971insT GRCh38
NC_000023.10:g.153581338_153581339insT , CM000685.1:g.153581338_153581339insT GRCh37
NC_000023.9:g.153234532_153234533insT NCBI36
NG_011506.1:g.26668_26669insA
NG_011506.2:g.26668_26669insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.6202+30_6202+31insA ENSP00000353467.4:n.6202+30_6202+31insA
ENST00000369850.10:c.6226+30_6226+31insA MANE Select ENSP00000358866.3:n.6226+30_6226+31insA
ENST00000369856.8:c.6145+30_6145+31insA ENSP00000358872.4:n.6145+30_6145+31insA
ENST00000422373.6:c.3161-296_3161-295insA ENSP00000416926.2:n.3161-296_3161-295insA
ENST00000610817.5:c.6283+30_6283+31insA ENSP00000480593.2:n.6283+30_6283+31insA
ENST00000673639.2:c.280-4281_280-4280insA
ENST00000676696.1:c.6505+30_6505+31insA ENSP00000503392.1:n.6505+30_6505+31insA
ENST00000678304.1:n.1405+30_1405+31insA
ENST00000344736.8:c.6106+30_6106+31insA ENSP00000358863.3:n.6106+30_6106+31insA
ENST00000360319.8:c.6202+30_6202+31insA ENSP00000353467.4:n.6202+30_6202+31insA
ENST00000369850.7:c.6226+30_6226+31insA ENSP00000358866.3:n.6226+30_6226+31insA
ENST00000369856.7:c.6145+30_6145+31insA ENSP00000358872.4:n.6145+30_6145+31insA
ENST00000415241.1:c.428+30_428+31insA
ENST00000420627.5:c.6182+30_6182+31insA ENSP00000408921.1:n.6182+30_6182+31insA
ENST00000422373.5:c.6202+30_6202+31insA ENSP00000416926.1:n.6202+30_6202+31insA
ENST00000444578.1:c.169+30_169+31insA ENSP00000397824.1:n.169+30_169+31insA
ENST00000466325.1:n.395_396insA
ENST00000490936.5:n.2215+30_2215+31insA
ENST00000610817.4:c.5844+422_5844+423insA ENSP00000480593.1:n.5844+422_5844+423insA
NM_001110556.1:c.6226+30_6226+31insA NP_001104026.1:n.6226+30_6226+31insA
NM_001456.3:c.6202+30_6202+31insA NP_001447.2:n.6202+30_6202+31insA
XM_011531127.1:c.6130+30_6130+31insA XP_011529429.1:n.6130+30_6130+31insA
XM_011531128.1:c.6106+30_6106+31insA XP_011529430.1:n.6106+30_6106+31insA
XM_011531129.1:c.6052+30_6052+31insA XP_011529431.1:n.6052+30_6052+31insA
XM_011531130.1:c.6028+30_6028+31insA XP_011529432.1:n.6028+30_6028+31insA
XM_011531131.1:c.6025+30_6025+31insA XP_011529433.1:n.6025+30_6025+31insA
NM_001110556.2:c.6226+30_6226+31insA MANE Select NP_001104026.1:n.6226+30_6226+31insA
NM_001456.4:c.6202+30_6202+31insA NP_001447.2:n.6202+30_6202+31insA