Canonical Allele Identifier: CA415198343

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353442C>T , CM000685.2:g.154353442C>T	GRCh38
NC_000023.10:g.153581810C>T , CM000685.1:g.153581810C>T	GRCh37
NC_000023.9:g.153235004C>T	NCBI36
NG_011506.1:g.26197G>A
NG_011506.2:g.26197G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001110556.2:c.5876G>A MANE Select	NP_001104026.1:p.Arg1959His
ENST00000369850.10:c.5876G>A MANE Select	ENSP00000358866.3:p.Arg1959His
NM_001110556.1:c.5876G>A	NP_001104026.1:p.Arg1959His
NM_001456.3:c.5852G>A	NP_001447.2:p.Arg1951His
NM_001456.4:c.5852G>A	NP_001447.2:p.Arg1951His
ENST00000344736.8:c.5756G>A	ENSP00000358863.3:p.Arg1919His
ENST00000360319.8:c.5852G>A	ENSP00000353467.4:p.Arg1951His
ENST00000360319.9:c.5852G>A	ENSP00000353467.4:p.Arg1951His
ENST00000369850.7:c.5876G>A	ENSP00000358866.3:p.Arg1959His
ENST00000369856.7:c.5795G>A	ENSP00000358872.4:p.Arg1932His
ENST00000369856.8:c.5795G>A	ENSP00000358872.4:p.Arg1932His
ENST00000415241.1:c.61G>A
ENST00000420627.5:c.5832G>A	ENSP00000408921.1:n.5832G>A
ENST00000422373.5:c.5852G>A	ENSP00000416926.1:p.Arg1951His
ENST00000422373.6:c.3161-767G>A	ENSP00000416926.2:n.3161-767G>A
ENST00000438732.2:c.550G>A
ENST00000466325.1:n.15G>A
ENST00000490936.5:n.1865G>A
ENST00000610817.4:c.5795G>A	ENSP00000480593.1:p.Arg1932His
ENST00000610817.5:c.5933G>A	ENSP00000480593.2:n.5933G>A
ENST00000673639.2:c.280-4752G>A
ENST00000676696.1:c.6155G>A	ENSP00000503392.1:n.6155G>A
ENST00000678304.1:n.1055G>A
XM_011531127.1:c.5780G>A	XP_011529429.1:p.Arg1927His
XM_011531128.1:c.5756G>A	XP_011529430.1:p.Arg1919His
XM_011531129.1:c.5702G>A	XP_011529431.1:p.Arg1901His
XM_011531130.1:c.5678G>A	XP_011529432.1:p.Arg1893His
XM_011531131.1:c.5675G>A	XP_011529433.1:p.Arg1892His