Canonical Allele Identifier: CA2466653201

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353112_154353115delinsTCAC , CM000685.2:g.154353112_154353115delinsTCAC	GRCh38
NC_000023.10:g.153581480_153581483delinsTCAC , CM000685.1:g.153581480_153581483delinsTCAC	GRCh37
NC_000023.9:g.153234674_153234677delinsTCAC	NCBI36
NG_011506.1:g.26524_26527delinsGTGA
NG_011506.2:g.26524_26527delinsGTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6088_6091delinsGTGA	ENSP00000353467.4:p.Val2030=
ENST00000369850.10:c.6112_6115delinsGTGA MANE Select	ENSP00000358866.3:p.Val2038=
ENST00000369856.8:c.6031_6034delinsGTGA	ENSP00000358872.4:p.Val2011=
ENST00000422373.6:c.3161-440_3161-437delinsGTGA	ENSP00000416926.2:n.3161-440_3161-437delinsGTGA
ENST00000610817.5:c.6169_6172delinsGTGA	ENSP00000480593.2:n.6169_6172delinsGTGA
ENST00000673639.2:c.280-4425_280-4422delinsGTGA
ENST00000676696.1:c.6391_6394delinsGTGA	ENSP00000503392.1:n.6391_6394delinsGTGA
ENST00000678304.1:n.1291_1294delinsGTGA
ENST00000344736.8:c.5992_5995delinsGTGA	ENSP00000358863.3:p.Val1998=
ENST00000360319.8:c.6088_6091delinsGTGA	ENSP00000353467.4:p.Val2030=
ENST00000369850.7:c.6112_6115delinsGTGA	ENSP00000358866.3:p.Val2038=
ENST00000369856.7:c.6031_6034delinsGTGA	ENSP00000358872.4:p.Val2011=
ENST00000415241.1:c.314_317delinsGTGA
ENST00000420627.5:c.6068_6071delinsGTGA	ENSP00000408921.1:n.6068_6071delinsGTGA
ENST00000422373.5:c.6088_6091delinsGTGA	ENSP00000416926.1:p.Val2030=
ENST00000444578.1:c.55_58delinsGTGA	ENSP00000397824.1:p.Val19=
ENST00000466325.1:n.251_254delinsGTGA
ENST00000490936.5:n.2101_2104delinsGTGA
ENST00000610817.4:c.5844+278_5844+281delinsGTGA	ENSP00000480593.1:n.5844+278_5844+281delinsGTGA
NM_001110556.1:c.6112_6115delinsGTGA	NP_001104026.1:p.Val2038=
NM_001456.3:c.6088_6091delinsGTGA	NP_001447.2:p.Val2030=
XM_011531127.1:c.6016_6019delinsGTGA	XP_011529429.1:p.Val2006=
XM_011531128.1:c.5992_5995delinsGTGA	XP_011529430.1:p.Val1998=
XM_011531129.1:c.5938_5941delinsGTGA	XP_011529431.1:p.Val1980=
XM_011531130.1:c.5914_5917delinsGTGA	XP_011529432.1:p.Val1972=
XM_011531131.1:c.5911_5914delinsGTGA	XP_011529433.1:p.Val1971=
NM_001110556.2:c.6112_6115delinsGTGA MANE Select	NP_001104026.1:p.Val2038=
NM_001456.4:c.6088_6091delinsGTGA	NP_001447.2:p.Val2030=