Canonical Allele Identifier: CA2559803738

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352754_154352755insAGGTGTGTG , CM000685.2:g.154352754_154352755insAGGTGTGTG	GRCh38
NC_000023.10:g.153581122_153581123insAGGTGTGTG , CM000685.1:g.153581122_153581123insAGGTGTGTG	GRCh37
NC_000023.9:g.153234316_153234317insAGGTGTGTG	NCBI36
NG_011506.1:g.26884_26885insCACACACCT
NG_011506.2:g.26884_26885insCACACACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6355+17_6355+18insCACACACCT	ENSP00000353467.4:n.6355+17_6355+18insCACACACCT
ENST00000369850.10:c.6379+17_6379+18insCACACACCT MANE Select	ENSP00000358866.3:n.6379+17_6379+18insCACACACCT
ENST00000369856.8:c.6298+17_6298+18insCACACACCT	ENSP00000358872.4:n.6298+17_6298+18insCACACACCT
ENST00000422373.6:c.3161-80_3161-79insCACACACCT	ENSP00000416926.2:n.3161-80_3161-79insCACACACCT
ENST00000610817.5:c.6436+17_6436+18insCACACACCT	ENSP00000480593.2:n.6436+17_6436+18insCACACACCT
ENST00000673639.2:c.280-4065_280-4064insCACACACCT
ENST00000676696.1:c.6658+17_6658+18insCACACACCT	ENSP00000503392.1:n.6658+17_6658+18insCACACACCT
ENST00000678304.1:n.1558+17_1558+18insCACACACCT
ENST00000344736.8:c.6259+17_6259+18insCACACACCT	ENSP00000358863.3:n.6259+17_6259+18insCACACACCT
ENST00000360319.8:c.6355+17_6355+18insCACACACCT	ENSP00000353467.4:n.6355+17_6355+18insCACACACCT
ENST00000369850.7:c.6379+17_6379+18insCACACACCT	ENSP00000358866.3:n.6379+17_6379+18insCACACACCT
ENST00000369856.7:c.6298+17_6298+18insCACACACCT	ENSP00000358872.4:n.6298+17_6298+18insCACACACCT
ENST00000415241.1:c.581+17_581+18insCACACACCT
ENST00000420627.5:c.6335+17_6335+18insCACACACCT	ENSP00000408921.1:n.6335+17_6335+18insCACACACCT
ENST00000422373.5:c.6355+17_6355+18insCACACACCT	ENSP00000416926.1:n.6355+17_6355+18insCACACACCT
ENST00000444578.1:c.322+17_322+18insCACACACCT	ENSP00000397824.1:n.322+17_322+18insCACACACCT
ENST00000466325.1:n.611_612insCACACACCT
ENST00000474358.5:n.12+17_12+18insCACACACCT
ENST00000490936.5:n.2368+17_2368+18insCACACACCT
ENST00000498411.1:n.67+62_67+63insCACACACCT
ENST00000610817.4:c.5844+638_5844+639insCACACACCT	ENSP00000480593.1:n.5844+638_5844+639insCACACACCT
NM_001110556.1:c.6379+17_6379+18insCACACACCT	NP_001104026.1:n.6379+17_6379+18insCACACACCT
NM_001456.3:c.6355+17_6355+18insCACACACCT	NP_001447.2:n.6355+17_6355+18insCACACACCT
XM_011531127.1:c.6283+17_6283+18insCACACACCT	XP_011529429.1:n.6283+17_6283+18insCACACACCT
XM_011531128.1:c.6259+17_6259+18insCACACACCT	XP_011529430.1:n.6259+17_6259+18insCACACACCT
XM_011531129.1:c.6205+17_6205+18insCACACACCT	XP_011529431.1:n.6205+17_6205+18insCACACACCT
XM_011531130.1:c.6181+17_6181+18insCACACACCT	XP_011529432.1:n.6181+17_6181+18insCACACACCT
XM_011531131.1:c.6178+17_6178+18insCACACACCT	XP_011529433.1:n.6178+17_6178+18insCACACACCT
NM_001110556.2:c.6379+17_6379+18insCACACACCT MANE Select	NP_001104026.1:n.6379+17_6379+18insCACACACCT
NM_001456.4:c.6355+17_6355+18insCACACACCT	NP_001447.2:n.6355+17_6355+18insCACACACCT