Canonical Allele Identifier: CA2531186719
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154352969_154352970insA , CM000685.2:g.154352969_154352970insA GRCh38
NC_000023.10:g.153581337_153581338insA , CM000685.1:g.153581337_153581338insA GRCh37
NC_000023.9:g.153234531_153234532insA NCBI36
NG_011506.1:g.26669_26670insT
NG_011506.2:g.26669_26670insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.6202+31_6202+32insT ENSP00000353467.4:n.6202+31_6202+32insT
ENST00000369850.10:c.6226+31_6226+32insT MANE Select ENSP00000358866.3:n.6226+31_6226+32insT
ENST00000369856.8:c.6145+31_6145+32insT ENSP00000358872.4:n.6145+31_6145+32insT
ENST00000422373.6:c.3161-295_3161-294insT ENSP00000416926.2:n.3161-295_3161-294insT
ENST00000610817.5:c.6283+31_6283+32insT ENSP00000480593.2:n.6283+31_6283+32insT
ENST00000673639.2:c.280-4280_280-4279insT
ENST00000676696.1:c.6505+31_6505+32insT ENSP00000503392.1:n.6505+31_6505+32insT
ENST00000678304.1:n.1405+31_1405+32insT
ENST00000344736.8:c.6106+31_6106+32insT ENSP00000358863.3:n.6106+31_6106+32insT
ENST00000360319.8:c.6202+31_6202+32insT ENSP00000353467.4:n.6202+31_6202+32insT
ENST00000369850.7:c.6226+31_6226+32insT ENSP00000358866.3:n.6226+31_6226+32insT
ENST00000369856.7:c.6145+31_6145+32insT ENSP00000358872.4:n.6145+31_6145+32insT
ENST00000415241.1:c.428+31_428+32insT
ENST00000420627.5:c.6182+31_6182+32insT ENSP00000408921.1:n.6182+31_6182+32insT
ENST00000422373.5:c.6202+31_6202+32insT ENSP00000416926.1:n.6202+31_6202+32insT
ENST00000444578.1:c.169+31_169+32insT ENSP00000397824.1:n.169+31_169+32insT
ENST00000466325.1:n.396_397insT
ENST00000490936.5:n.2215+31_2215+32insT
ENST00000610817.4:c.5844+423_5844+424insT ENSP00000480593.1:n.5844+423_5844+424insT
NM_001110556.1:c.6226+31_6226+32insT NP_001104026.1:n.6226+31_6226+32insT
NM_001456.3:c.6202+31_6202+32insT NP_001447.2:n.6202+31_6202+32insT
XM_011531127.1:c.6130+31_6130+32insT XP_011529429.1:n.6130+31_6130+32insT
XM_011531128.1:c.6106+31_6106+32insT XP_011529430.1:n.6106+31_6106+32insT
XM_011531129.1:c.6052+31_6052+32insT XP_011529431.1:n.6052+31_6052+32insT
XM_011531130.1:c.6028+31_6028+32insT XP_011529432.1:n.6028+31_6028+32insT
XM_011531131.1:c.6025+31_6025+32insT XP_011529433.1:n.6025+31_6025+32insT
NM_001110556.2:c.6226+31_6226+32insT MANE Select NP_001104026.1:n.6226+31_6226+32insT
NM_001456.4:c.6202+31_6202+32insT NP_001447.2:n.6202+31_6202+32insT