Canonical Allele Identifier: CA2525423099

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352966_154352967insGT , CM000685.2:g.154352966_154352967insGT	GRCh38
NC_000023.10:g.153581334_153581335insGT , CM000685.1:g.153581334_153581335insGT	GRCh37
NC_000023.9:g.153234528_153234529insGT	NCBI36
NG_011506.1:g.26672_26673insAC
NG_011506.2:g.26672_26673insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6202+34_6202+35insAC	ENSP00000353467.4:n.6202+34_6202+35insAC
ENST00000369850.10:c.6226+34_6226+35insAC MANE Select	ENSP00000358866.3:n.6226+34_6226+35insAC
ENST00000369856.8:c.6145+34_6145+35insAC	ENSP00000358872.4:n.6145+34_6145+35insAC
ENST00000422373.6:c.3161-292_3161-291insAC	ENSP00000416926.2:n.3161-292_3161-291insAC
ENST00000610817.5:c.6283+34_6283+35insAC	ENSP00000480593.2:n.6283+34_6283+35insAC
ENST00000673639.2:c.280-4277_280-4276insAC
ENST00000676696.1:c.6505+34_6505+35insAC	ENSP00000503392.1:n.6505+34_6505+35insAC
ENST00000678304.1:n.1405+34_1405+35insAC
ENST00000344736.8:c.6106+34_6106+35insAC	ENSP00000358863.3:n.6106+34_6106+35insAC
ENST00000360319.8:c.6202+34_6202+35insAC	ENSP00000353467.4:n.6202+34_6202+35insAC
ENST00000369850.7:c.6226+34_6226+35insAC	ENSP00000358866.3:n.6226+34_6226+35insAC
ENST00000369856.7:c.6145+34_6145+35insAC	ENSP00000358872.4:n.6145+34_6145+35insAC
ENST00000415241.1:c.428+34_428+35insAC
ENST00000420627.5:c.6182+34_6182+35insAC	ENSP00000408921.1:n.6182+34_6182+35insAC
ENST00000422373.5:c.6202+34_6202+35insAC	ENSP00000416926.1:n.6202+34_6202+35insAC
ENST00000444578.1:c.169+34_169+35insAC	ENSP00000397824.1:n.169+34_169+35insAC
ENST00000466325.1:n.399_400insAC
ENST00000490936.5:n.2215+34_2215+35insAC
ENST00000610817.4:c.5844+426_5844+427insAC	ENSP00000480593.1:n.5844+426_5844+427insAC
NM_001110556.1:c.6226+34_6226+35insAC	NP_001104026.1:n.6226+34_6226+35insAC
NM_001456.3:c.6202+34_6202+35insAC	NP_001447.2:n.6202+34_6202+35insAC
XM_011531127.1:c.6130+34_6130+35insAC	XP_011529429.1:n.6130+34_6130+35insAC
XM_011531128.1:c.6106+34_6106+35insAC	XP_011529430.1:n.6106+34_6106+35insAC
XM_011531129.1:c.6052+34_6052+35insAC	XP_011529431.1:n.6052+34_6052+35insAC
XM_011531130.1:c.6028+34_6028+35insAC	XP_011529432.1:n.6028+34_6028+35insAC
XM_011531131.1:c.6025+34_6025+35insAC	XP_011529433.1:n.6025+34_6025+35insAC
NM_001110556.2:c.6226+34_6226+35insAC MANE Select	NP_001104026.1:n.6226+34_6226+35insAC
NM_001456.4:c.6202+34_6202+35insAC	NP_001447.2:n.6202+34_6202+35insAC