Canonical Allele Identifier: CA2562922865

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352936_154352937insGCCA , CM000685.2:g.154352936_154352937insGCCA	GRCh38
NC_000023.10:g.153581304_153581305insGCCA , CM000685.1:g.153581304_153581305insGCCA	GRCh37
NC_000023.9:g.153234498_153234499insGCCA	NCBI36
NG_011506.1:g.26703_26704insGGCT
NG_011506.2:g.26703_26704insGGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6203-12_6203-11insGGCT	ENSP00000353467.4:n.6203-12_6203-11insGGCT
ENST00000369850.10:c.6227-12_6227-11insGGCT MANE Select	ENSP00000358866.3:n.6227-12_6227-11insGGCT
ENST00000369856.8:c.6146-12_6146-11insGGCT	ENSP00000358872.4:n.6146-12_6146-11insGGCT
ENST00000422373.6:c.3161-261_3161-260insGGCT	ENSP00000416926.2:n.3161-261_3161-260insGGCT
ENST00000610817.5:c.6284-12_6284-11insGGCT	ENSP00000480593.2:n.6284-12_6284-11insGGCT
ENST00000673639.2:c.280-4246_280-4245insGGCT
ENST00000676696.1:c.6506-12_6506-11insGGCT	ENSP00000503392.1:n.6506-12_6506-11insGGCT
ENST00000678304.1:n.1406-12_1406-11insGGCT
ENST00000344736.8:c.6107-12_6107-11insGGCT	ENSP00000358863.3:n.6107-12_6107-11insGGCT
ENST00000360319.8:c.6203-12_6203-11insGGCT	ENSP00000353467.4:n.6203-12_6203-11insGGCT
ENST00000369850.7:c.6227-12_6227-11insGGCT	ENSP00000358866.3:n.6227-12_6227-11insGGCT
ENST00000369856.7:c.6146-12_6146-11insGGCT	ENSP00000358872.4:n.6146-12_6146-11insGGCT
ENST00000415241.1:c.429-12_429-11insGGCT
ENST00000420627.5:c.6183-12_6183-11insGGCT	ENSP00000408921.1:n.6183-12_6183-11insGGCT
ENST00000422373.5:c.6203-12_6203-11insGGCT	ENSP00000416926.1:n.6203-12_6203-11insGGCT
ENST00000444578.1:c.170-12_170-11insGGCT	ENSP00000397824.1:n.170-12_170-11insGGCT
ENST00000466325.1:n.430_431insGGCT
ENST00000490936.5:n.2216-12_2216-11insGGCT
ENST00000610817.4:c.5844+457_5844+458insGGCT	ENSP00000480593.1:n.5844+457_5844+458insGGCT
NM_001110556.1:c.6227-12_6227-11insGGCT	NP_001104026.1:n.6227-12_6227-11insGGCT
NM_001456.3:c.6203-12_6203-11insGGCT	NP_001447.2:n.6203-12_6203-11insGGCT
XM_011531127.1:c.6131-12_6131-11insGGCT	XP_011529429.1:n.6131-12_6131-11insGGCT
XM_011531128.1:c.6107-12_6107-11insGGCT	XP_011529430.1:n.6107-12_6107-11insGGCT
XM_011531129.1:c.6053-12_6053-11insGGCT	XP_011529431.1:n.6053-12_6053-11insGGCT
XM_011531130.1:c.6029-12_6029-11insGGCT	XP_011529432.1:n.6029-12_6029-11insGGCT
XM_011531131.1:c.6026-12_6026-11insGGCT	XP_011529433.1:n.6026-12_6026-11insGGCT
NM_001110556.2:c.6227-12_6227-11insGGCT MANE Select	NP_001104026.1:n.6227-12_6227-11insGGCT
NM_001456.4:c.6203-12_6203-11insGGCT	NP_001447.2:n.6203-12_6203-11insGGCT