Canonical Allele Identifier: CA415192291

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153580991G>C (hg19) ; chrX:g.154352623G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352623G>C , CM000685.2:g.154352623G>C	GRCh38
NC_000023.10:g.153580991G>C , CM000685.1:g.153580991G>C	GRCh37
NC_000023.9:g.153234185G>C	NCBI36
NG_011506.1:g.27016C>G
NG_011506.2:g.27016C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6408C>G	ENSP00000353467.4:p.Ile2136Met
ENST00000369850.10:c.6432C>G MANE Select	ENSP00000358866.3:p.Ile2144Met
ENST00000369856.8:c.6351C>G	ENSP00000358872.4:p.Ile2117Met
ENST00000422373.6:c.3213C>G	ENSP00000416926.2:p.Ile1071Met
ENST00000610817.5:c.6489C>G	ENSP00000480593.2:n.6489C>G
ENST00000673639.2:c.280-3933C>G
ENST00000676696.1:c.6711C>G	ENSP00000503392.1:n.6711C>G
ENST00000678304.1:n.1611C>G
ENST00000344736.8:c.6312C>G	ENSP00000358863.3:p.Ile2104Met
ENST00000360319.8:c.6408C>G	ENSP00000353467.4:p.Ile2136Met
ENST00000369850.7:c.6432C>G	ENSP00000358866.3:p.Ile2144Met
ENST00000369856.7:c.6351C>G	ENSP00000358872.4:p.Ile2117Met
ENST00000415241.1:c.634C>G
ENST00000420627.5:c.6388C>G	ENSP00000408921.1:n.6388C>G
ENST00000422373.5:c.6408C>G	ENSP00000416926.1:p.Ile2136Met
ENST00000444578.1:c.322+149C>G	ENSP00000397824.1:n.322+149C>G
ENST00000466325.1:n.743C>G
ENST00000474358.5:n.65C>G
ENST00000490936.5:n.2421C>G
ENST00000498411.1:n.67+194C>G
ENST00000610817.4:c.5845-673C>G	ENSP00000480593.1:n.5845-673C>G
NM_001110556.1:c.6432C>G	NP_001104026.1:p.Ile2144Met
NM_001456.3:c.6408C>G	NP_001447.2:p.Ile2136Met
XM_011531127.1:c.6336C>G	XP_011529429.1:p.Ile2112Met
XM_011531128.1:c.6312C>G	XP_011529430.1:p.Ile2104Met
XM_011531129.1:c.6258C>G	XP_011529431.1:p.Ile2086Met
XM_011531130.1:c.6234C>G	XP_011529432.1:p.Ile2078Met
XM_011531131.1:c.6231C>G	XP_011529433.1:p.Ile2077Met
NM_001110556.2:c.6432C>G MANE Select	NP_001104026.1:p.Ile2144Met
NM_001456.4:c.6408C>G	NP_001447.2:p.Ile2136Met