Canonical Allele Identifier: CA415199102

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353592T>C , CM000685.2:g.154353592T>C	GRCh38
NC_000023.10:g.153581960T>C , CM000685.1:g.153581960T>C	GRCh37
NC_000023.9:g.153235154T>C	NCBI36
NG_011506.1:g.26047A>G
NG_011506.2:g.26047A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5798A>G	ENSP00000353467.4:p.Gln1933Arg
ENST00000369850.10:c.5822A>G MANE Select	ENSP00000358866.3:p.Gln1941Arg
ENST00000369856.8:c.5741A>G	ENSP00000358872.4:p.Gln1914Arg
ENST00000422373.6:c.3161-917A>G	ENSP00000416926.2:n.3161-917A>G
ENST00000610817.5:c.5879A>G	ENSP00000480593.2:n.5879A>G
ENST00000673639.2:c.280-4902A>G
ENST00000676696.1:c.6101A>G	ENSP00000503392.1:n.6101A>G
ENST00000678304.1:n.1001A>G
ENST00000344736.8:c.5702A>G	ENSP00000358863.3:p.Gln1901Arg
ENST00000360319.8:c.5798A>G	ENSP00000353467.4:p.Gln1933Arg
ENST00000369850.7:c.5822A>G	ENSP00000358866.3:p.Gln1941Arg
ENST00000369856.7:c.5741A>G	ENSP00000358872.4:p.Gln1914Arg
ENST00000415241.1:c.7A>G
ENST00000420627.5:c.5778A>G	ENSP00000408921.1:n.5778A>G
ENST00000422373.5:c.5798A>G	ENSP00000416926.1:p.Gln1933Arg
ENST00000438732.2:c.535-135A>G
ENST00000490936.5:n.1811A>G
ENST00000610817.4:c.5741A>G	ENSP00000480593.1:p.Gln1914Arg
NM_001110556.1:c.5822A>G	NP_001104026.1:p.Gln1941Arg
NM_001456.3:c.5798A>G	NP_001447.2:p.Gln1933Arg
XM_011531127.1:c.5726A>G	XP_011529429.1:p.Gln1909Arg
XM_011531128.1:c.5702A>G	XP_011529430.1:p.Gln1901Arg
XM_011531129.1:c.5687-135A>G	XP_011529431.1:n.5687-135A>G
XM_011531130.1:c.5663-135A>G	XP_011529432.1:n.5663-135A>G
XM_011531131.1:c.5621A>G	XP_011529433.1:p.Gln1874Arg
NM_001110556.2:c.5822A>G MANE Select	NP_001104026.1:p.Gln1941Arg
NM_001456.4:c.5798A>G	NP_001447.2:p.Gln1933Arg