Canonical Allele Identifier: CA10559931

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350109G>C , CM000685.2:g.154350109G>C	GRCh38
NC_000023.10:g.153578477G>C , CM000685.1:g.153578477G>C	GRCh37
NC_000023.9:g.153231671G>C	NCBI36
NG_011506.1:g.29530C>G
NG_011506.2:g.29530C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001110556.2:c.7255C>G MANE Select	NP_001104026.1:p.Arg2419Gly
ENST00000369850.10:c.7255C>G MANE Select	ENSP00000358866.3:p.Arg2419Gly
NM_001110556.1:c.7255C>G	NP_001104026.1:p.Arg2419Gly
NM_001456.3:c.7231C>G	NP_001447.2:p.Arg2411Gly
NM_001456.4:c.7231C>G	NP_001447.2:p.Arg2411Gly
ENST00000344736.8:c.7135C>G	ENSP00000358863.3:p.Arg2379Gly
ENST00000360319.8:c.7231C>G	ENSP00000353467.4:p.Arg2411Gly
ENST00000360319.9:c.7231C>G	ENSP00000353467.4:p.Arg2411Gly
ENST00000369850.7:c.7255C>G	ENSP00000358866.3:p.Arg2419Gly
ENST00000369856.7:c.7174C>G	ENSP00000358872.4:p.Arg2392Gly
ENST00000369856.8:c.7174C>G	ENSP00000358872.4:p.Arg2392Gly
ENST00000420627.5:c.7211C>G	ENSP00000408921.1:n.7211C>G
ENST00000422373.5:c.7231C>G	ENSP00000416926.1:p.Arg2411Gly
ENST00000422373.6:c.4036C>G	ENSP00000416926.2:p.Arg1346Gly
ENST00000462590.1:n.247C>G
ENST00000490936.5:n.4484C>G
ENST00000498411.1:n.68-1279C>G
ENST00000498491.5:n.296C>G
ENST00000610817.4:c.6259C>G	ENSP00000480593.1:p.Arg2087Gly
ENST00000610817.5:c.7312C>G	ENSP00000480593.2:n.7312C>G
ENST00000673639.2:c.280-1419C>G
ENST00000676696.1:c.7534C>G	ENSP00000503392.1:n.7534C>G
ENST00000678304.1:n.2973C>G
XM_011531127.1:c.7159C>G	XP_011529429.1:p.Arg2387Gly
XM_011531128.1:c.7135C>G	XP_011529430.1:p.Arg2379Gly
XM_011531129.1:c.7081C>G	XP_011529431.1:p.Arg2361Gly
XM_011531130.1:c.7057C>G	XP_011529432.1:p.Arg2353Gly
XM_011531131.1:c.7054C>G	XP_011529433.1:p.Arg2352Gly