Canonical Allele Identifier: CA2466653236

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353212_154353214delinsCAG , CM000685.2:g.154353212_154353214delinsCAG	GRCh38
NC_000023.10:g.153581580_153581582delinsCAG , CM000685.1:g.153581580_153581582delinsCAG	GRCh37
NC_000023.9:g.153234774_153234776delinsCAG	NCBI36
NG_011506.1:g.26425_26427delinsCTG
NG_011506.2:g.26425_26427delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5999-10_5999-8delinsCTG	ENSP00000353467.4:n.5999-10_5999-8delinsCTG
ENST00000369850.10:c.6023-10_6023-8delinsCTG MANE Select	ENSP00000358866.3:n.6023-10_6023-8delinsCTG
ENST00000369856.8:c.5942-10_5942-8delinsCTG	ENSP00000358872.4:n.5942-10_5942-8delinsCTG
ENST00000422373.6:c.3161-539_3161-537delinsCTG	ENSP00000416926.2:n.3161-539_3161-537delinsCTG
ENST00000610817.5:c.6080-10_6080-8delinsCTG	ENSP00000480593.2:n.6080-10_6080-8delinsCTG
ENST00000673639.2:c.280-4524_280-4522delinsCTG
ENST00000676696.1:c.6302-10_6302-8delinsCTG	ENSP00000503392.1:n.6302-10_6302-8delinsCTG
ENST00000678304.1:n.1202-10_1202-8delinsCTG
ENST00000344736.8:c.5903-10_5903-8delinsCTG	ENSP00000358863.3:n.5903-10_5903-8delinsCTG
ENST00000360319.8:c.5999-10_5999-8delinsCTG	ENSP00000353467.4:n.5999-10_5999-8delinsCTG
ENST00000369850.7:c.6023-10_6023-8delinsCTG	ENSP00000358866.3:n.6023-10_6023-8delinsCTG
ENST00000369856.7:c.5942-10_5942-8delinsCTG	ENSP00000358872.4:n.5942-10_5942-8delinsCTG
ENST00000415241.1:c.215_217delinsCTG
ENST00000420627.5:c.5979-10_5979-8delinsCTG	ENSP00000408921.1:n.5979-10_5979-8delinsCTG
ENST00000422373.5:c.5999-10_5999-8delinsCTG	ENSP00000416926.1:n.5999-10_5999-8delinsCTG
ENST00000466325.1:n.162-10_162-8delinsCTG
ENST00000490936.5:n.2012-10_2012-8delinsCTG
ENST00000610817.4:c.5844+179_5844+181delinsCTG	ENSP00000480593.1:n.5844+179_5844+181delinsCTG
NM_001110556.1:c.6023-10_6023-8delinsCTG	NP_001104026.1:n.6023-10_6023-8delinsCTG
NM_001456.3:c.5999-10_5999-8delinsCTG	NP_001447.2:n.5999-10_5999-8delinsCTG
XM_011531127.1:c.5927-10_5927-8delinsCTG	XP_011529429.1:n.5927-10_5927-8delinsCTG
XM_011531128.1:c.5903-10_5903-8delinsCTG	XP_011529430.1:n.5903-10_5903-8delinsCTG
XM_011531129.1:c.5849-10_5849-8delinsCTG	XP_011529431.1:n.5849-10_5849-8delinsCTG
XM_011531130.1:c.5825-10_5825-8delinsCTG	XP_011529432.1:n.5825-10_5825-8delinsCTG
XM_011531131.1:c.5822-10_5822-8delinsCTG	XP_011529433.1:n.5822-10_5822-8delinsCTG
NM_001110556.2:c.6023-10_6023-8delinsCTG MANE Select	NP_001104026.1:n.6023-10_6023-8delinsCTG
NM_001456.4:c.5999-10_5999-8delinsCTG	NP_001447.2:n.5999-10_5999-8delinsCTG