Canonical Allele Identifier: CA2466655324

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154358708_154358709delinsAC , CM000685.2:g.154358708_154358709delinsAC	GRCh38
NC_000023.10:g.153587076_153587077delinsAC , CM000685.1:g.153587076_153587077delinsAC	GRCh37
NC_000023.9:g.153240270_153240271delinsAC	NCBI36
NG_011506.1:g.20930_20931delinsGT
NG_011506.2:g.20930_20931delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.4475-141_4475-140delinsGT	ENSP00000353467.4:n.4475-141_4475-140delinsGT
ENST00000369850.10:c.4475-141_4475-140delinsGT MANE Select	ENSP00000358866.3:n.4475-141_4475-140delinsGT
ENST00000369856.8:c.4394-141_4394-140delinsGT	ENSP00000358872.4:n.4394-141_4394-140delinsGT
ENST00000422373.6:c.3160+2646_3160+2647delinsGT	ENSP00000416926.2:n.3160+2646_3160+2647delinsGT
ENST00000610817.5:c.4532-141_4532-140delinsGT	ENSP00000480593.2:n.4532-141_4532-140delinsGT
ENST00000673639.2:c.279+6727_279+6728delinsGT
ENST00000676696.1:c.4754-141_4754-140delinsGT	ENSP00000503392.1:n.4754-141_4754-140delinsGT
ENST00000678304.1:n.148+380_148+381delinsGT
ENST00000344736.8:c.4475-141_4475-140delinsGT	ENSP00000358863.3:n.4475-141_4475-140delinsGT
ENST00000360319.8:c.4475-141_4475-140delinsGT	ENSP00000353467.4:n.4475-141_4475-140delinsGT
ENST00000369850.7:c.4475-141_4475-140delinsGT	ENSP00000358866.3:n.4475-141_4475-140delinsGT
ENST00000369856.7:c.4394-141_4394-140delinsGT	ENSP00000358872.4:n.4394-141_4394-140delinsGT
ENST00000420627.5:c.4431-141_4431-140delinsGT	ENSP00000408921.1:n.4431-141_4431-140delinsGT
ENST00000422373.5:c.4475-141_4475-140delinsGT	ENSP00000416926.1:n.4475-141_4475-140delinsGT
ENST00000490936.5:n.488-141_488-140delinsGT
ENST00000610817.4:c.4394-141_4394-140delinsGT	ENSP00000480593.1:n.4394-141_4394-140delinsGT
NM_001110556.1:c.4475-141_4475-140delinsGT	NP_001104026.1:n.4475-141_4475-140delinsGT
NM_001456.3:c.4475-141_4475-140delinsGT	NP_001447.2:n.4475-141_4475-140delinsGT
XM_011531127.1:c.4475-141_4475-140delinsGT	XP_011529429.1:n.4475-141_4475-140delinsGT
XM_011531128.1:c.4475-141_4475-140delinsGT	XP_011529430.1:n.4475-141_4475-140delinsGT
XM_011531129.1:c.4475-141_4475-140delinsGT	XP_011529431.1:n.4475-141_4475-140delinsGT
XM_011531130.1:c.4475-141_4475-140delinsGT	XP_011529432.1:n.4475-141_4475-140delinsGT
XM_011531131.1:c.4274-141_4274-140delinsGT	XP_011529433.1:n.4274-141_4274-140delinsGT
NM_001110556.2:c.4475-141_4475-140delinsGT MANE Select	NP_001104026.1:n.4475-141_4475-140delinsGT
NM_001456.4:c.4475-141_4475-140delinsGT	NP_001447.2:n.4475-141_4475-140delinsGT