Canonical Allele Identifier: CA2466653280

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353316_154353317delinsCG , CM000685.2:g.154353316_154353317delinsCG	GRCh38
NC_000023.10:g.153581684_153581685delinsCG , CM000685.1:g.153581684_153581685delinsCG	GRCh37
NC_000023.9:g.153234878_153234879delinsCG	NCBI36
NG_011506.1:g.26322_26323delinsCG
NG_011506.2:g.26322_26323delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5977_5978delinsCG	ENSP00000353467.4:p.Arg1993=
ENST00000369850.10:c.6001_6002delinsCG MANE Select	ENSP00000358866.3:p.Arg2001=
ENST00000369856.8:c.5920_5921delinsCG	ENSP00000358872.4:p.Arg1974=
ENST00000422373.6:c.3161-642_3161-641delinsCG	ENSP00000416926.2:n.3161-642_3161-641delinsCG
ENST00000610817.5:c.6058_6059delinsCG	ENSP00000480593.2:n.6058_6059delinsCG
ENST00000673639.2:c.280-4627_280-4626delinsCG
ENST00000676696.1:c.6280_6281delinsCG	ENSP00000503392.1:n.6280_6281delinsCG
ENST00000678304.1:n.1180_1181delinsCG
ENST00000344736.8:c.5881_5882delinsCG	ENSP00000358863.3:p.Arg1961=
ENST00000360319.8:c.5977_5978delinsCG	ENSP00000353467.4:p.Arg1993=
ENST00000369850.7:c.6001_6002delinsCG	ENSP00000358866.3:p.Arg2001=
ENST00000369856.7:c.5920_5921delinsCG	ENSP00000358872.4:p.Arg1974=
ENST00000415241.1:c.186_187delinsCG
ENST00000420627.5:c.5957_5958delinsCG	ENSP00000408921.1:n.5957_5958delinsCG
ENST00000422373.5:c.5977_5978delinsCG	ENSP00000416926.1:p.Arg1993=
ENST00000438732.2:c.675_676delinsCG
ENST00000466325.1:n.140_141delinsCG
ENST00000490936.5:n.1990_1991delinsCG
ENST00000610817.4:c.5844+76_5844+77delinsCG	ENSP00000480593.1:n.5844+76_5844+77delinsCG
NM_001110556.1:c.6001_6002delinsCG	NP_001104026.1:p.Arg2001=
NM_001456.3:c.5977_5978delinsCG	NP_001447.2:p.Arg1993=
XM_011531127.1:c.5905_5906delinsCG	XP_011529429.1:p.Arg1969=
XM_011531128.1:c.5881_5882delinsCG	XP_011529430.1:p.Arg1961=
XM_011531129.1:c.5827_5828delinsCG	XP_011529431.1:p.Arg1943=
XM_011531130.1:c.5803_5804delinsCG	XP_011529432.1:p.Arg1935=
XM_011531131.1:c.5800_5801delinsCG	XP_011529433.1:p.Arg1934=
NM_001110556.2:c.6001_6002delinsCG MANE Select	NP_001104026.1:p.Arg2001=
NM_001456.4:c.5977_5978delinsCG	NP_001447.2:p.Arg1993=