Canonical Allele Identifier: CA2466660330

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154370833_154370843delinsCCCCGCCCCCG , CM000685.2:g.154370833_154370843delinsCCCCGCCCCCG	GRCh38
NC_000023.10:g.153599201_153599211delinsCCCCGCCCCCG , CM000685.1:g.153599201_153599211delinsCCCCGCCCCCG	GRCh37
NC_000023.9:g.153252395_153252405delinsCCCCGCCCCCG	NCBI36
NG_008677.1:g.1406_1416delinsCCCCGCCCCCG , LRG_745:g.1406_1416delinsCCCCGCCCCCG
NG_011506.1:g.8796_8806delinsCGGGGGCGGGG
NG_011506.2:g.8796_8806delinsCGGGGGCGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.373+30_373+40delinsCGGGGGCGGGG	ENSP00000353467.4:n.373+30_373+40delinsCGGGGGCGGGG
ENST00000369850.10:c.373+30_373+40delinsCGGGGGCGGGG MANE Select	ENSP00000358866.3:n.373+30_373+40delinsCGGGGGCGGGG
ENST00000369856.8:c.292+30_292+40delinsCGGGGGCGGGG	ENSP00000358872.4:n.292+30_292+40delinsCGGGGGCGGGG
ENST00000422373.6:c.373+30_373+40delinsCGGGGGCGGGG	ENSP00000416926.2:n.373+30_373+40delinsCGGGGGCGGGG
ENST00000610817.5:c.373+30_373+40delinsCGGGGGCGGGG	ENSP00000480593.2:n.373+30_373+40delinsCGGGGGCGGGG
ENST00000676696.1:c.373+30_373+40delinsCGGGGGCGGGG	ENSP00000503392.1:n.373+30_373+40delinsCGGGGGCGGGG
ENST00000344736.8:c.373+30_373+40delinsCGGGGGCGGGG	ENSP00000358863.3:n.373+30_373+40delinsCGGGGGCGGGG
ENST00000360319.8:c.373+30_373+40delinsCGGGGGCGGGG	ENSP00000353467.4:n.373+30_373+40delinsCGGGGGCGGGG
ENST00000369850.7:c.373+30_373+40delinsCGGGGGCGGGG	ENSP00000358866.3:n.373+30_373+40delinsCGGGGGCGGGG
ENST00000369856.7:c.292+30_292+40delinsCGGGGGCGGGG	ENSP00000358872.4:n.292+30_292+40delinsCGGGGGCGGGG
ENST00000420627.5:c.331+30_331+40delinsCGGGGGCGGGG	ENSP00000408921.1:n.331+30_331+40delinsCGGGGGCGGGG
ENST00000422373.5:c.373+30_373+40delinsCGGGGGCGGGG	ENSP00000416926.1:n.373+30_373+40delinsCGGGGGCGGGG
ENST00000610817.4:c.292+30_292+40delinsCGGGGGCGGGG	ENSP00000480593.1:n.292+30_292+40delinsCGGGGGCGGGG
NM_001110556.1:c.373+30_373+40delinsCGGGGGCGGGG	NP_001104026.1:n.373+30_373+40delinsCGGGGGCGGGG
NM_001456.3:c.373+30_373+40delinsCGGGGGCGGGG	NP_001447.2:n.373+30_373+40delinsCGGGGGCGGGG
XM_011531127.1:c.373+30_373+40delinsCGGGGGCGGGG	XP_011529429.1:n.373+30_373+40delinsCGGGGGCGGGG
XM_011531128.1:c.373+30_373+40delinsCGGGGGCGGGG	XP_011529430.1:n.373+30_373+40delinsCGGGGGCGGGG
XM_011531129.1:c.373+30_373+40delinsCGGGGGCGGGG	XP_011529431.1:n.373+30_373+40delinsCGGGGGCGGGG
XM_011531130.1:c.373+30_373+40delinsCGGGGGCGGGG	XP_011529432.1:n.373+30_373+40delinsCGGGGGCGGGG
XM_011531131.1:c.373+30_373+40delinsCGGGGGCGGGG	XP_011529433.1:n.373+30_373+40delinsCGGGGGCGGGG
NM_001110556.2:c.373+30_373+40delinsCGGGGGCGGGG MANE Select	NP_001104026.1:n.373+30_373+40delinsCGGGGGCGGGG
NM_001456.4:c.373+30_373+40delinsCGGGGGCGGGG	NP_001447.2:n.373+30_373+40delinsCGGGGGCGGGG