Canonical Allele Identifier: CA2466653048

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352741_154352742delinsAG , CM000685.2:g.154352741_154352742delinsAG	GRCh38
NC_000023.10:g.153581109_153581110delinsAG , CM000685.1:g.153581109_153581110delinsAG	GRCh37
NC_000023.9:g.153234303_153234304delinsAG	NCBI36
NG_011506.1:g.26897_26898delinsCT
NG_011506.2:g.26897_26898delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6355+30_6355+31delinsCT	ENSP00000353467.4:n.6355+30_6355+31delinsCT
ENST00000369850.10:c.6379+30_6379+31delinsCT MANE Select	ENSP00000358866.3:n.6379+30_6379+31delinsCT
ENST00000369856.8:c.6298+30_6298+31delinsCT	ENSP00000358872.4:n.6298+30_6298+31delinsCT
ENST00000422373.6:c.3161-67_3161-66delinsCT	ENSP00000416926.2:n.3161-67_3161-66delinsCT
ENST00000610817.5:c.6436+30_6436+31delinsCT	ENSP00000480593.2:n.6436+30_6436+31delinsCT
ENST00000673639.2:c.280-4052_280-4051delinsCT
ENST00000676696.1:c.6658+30_6658+31delinsCT	ENSP00000503392.1:n.6658+30_6658+31delinsCT
ENST00000678304.1:n.1558+30_1558+31delinsCT
ENST00000344736.8:c.6259+30_6259+31delinsCT	ENSP00000358863.3:n.6259+30_6259+31delinsCT
ENST00000360319.8:c.6355+30_6355+31delinsCT	ENSP00000353467.4:n.6355+30_6355+31delinsCT
ENST00000369850.7:c.6379+30_6379+31delinsCT	ENSP00000358866.3:n.6379+30_6379+31delinsCT
ENST00000369856.7:c.6298+30_6298+31delinsCT	ENSP00000358872.4:n.6298+30_6298+31delinsCT
ENST00000415241.1:c.581+30_581+31delinsCT
ENST00000420627.5:c.6335+30_6335+31delinsCT	ENSP00000408921.1:n.6335+30_6335+31delinsCT
ENST00000422373.5:c.6355+30_6355+31delinsCT	ENSP00000416926.1:n.6355+30_6355+31delinsCT
ENST00000444578.1:c.322+30_322+31delinsCT	ENSP00000397824.1:n.322+30_322+31delinsCT
ENST00000466325.1:n.624_625delinsCT
ENST00000474358.5:n.12+30_12+31delinsCT
ENST00000490936.5:n.2368+30_2368+31delinsCT
ENST00000498411.1:n.67+75_67+76delinsCT
ENST00000610817.4:c.5844+651_5844+652delinsCT	ENSP00000480593.1:n.5844+651_5844+652delinsCT
NM_001110556.1:c.6379+30_6379+31delinsCT	NP_001104026.1:n.6379+30_6379+31delinsCT
NM_001456.3:c.6355+30_6355+31delinsCT	NP_001447.2:n.6355+30_6355+31delinsCT
XM_011531127.1:c.6283+30_6283+31delinsCT	XP_011529429.1:n.6283+30_6283+31delinsCT
XM_011531128.1:c.6259+30_6259+31delinsCT	XP_011529430.1:n.6259+30_6259+31delinsCT
XM_011531129.1:c.6205+30_6205+31delinsCT	XP_011529431.1:n.6205+30_6205+31delinsCT
XM_011531130.1:c.6181+30_6181+31delinsCT	XP_011529432.1:n.6181+30_6181+31delinsCT
XM_011531131.1:c.6178+30_6178+31delinsCT	XP_011529433.1:n.6178+30_6178+31delinsCT
NM_001110556.2:c.6379+30_6379+31delinsCT MANE Select	NP_001104026.1:n.6379+30_6379+31delinsCT
NM_001456.4:c.6355+30_6355+31delinsCT	NP_001447.2:n.6355+30_6355+31delinsCT