Canonical Allele Identifier: CA415184686

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153579284A>C (hg19) ; chrX:g.154350916A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350916A>C , CM000685.2:g.154350916A>C	GRCh38
NC_000023.10:g.153579284A>C , CM000685.1:g.153579284A>C	GRCh37
NC_000023.9:g.153232478A>C	NCBI36
NG_011506.1:g.28723T>G
NG_011506.2:g.28723T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.7125T>G	ENSP00000353467.4:p.Ile2375Met
ENST00000369850.10:c.7149T>G MANE Select	ENSP00000358866.3:p.Ile2383Met
ENST00000369856.8:c.7068T>G	ENSP00000358872.4:p.Ile2356Met
ENST00000422373.6:c.3930T>G	ENSP00000416926.2:p.Ile1310Met
ENST00000610817.5:c.7206T>G	ENSP00000480593.2:n.7206T>G
ENST00000673639.2:c.280-2226T>G
ENST00000676696.1:c.7428T>G	ENSP00000503392.1:n.7428T>G
ENST00000678304.1:n.2867T>G
ENST00000344736.8:c.7029T>G	ENSP00000358863.3:p.Ile2343Met
ENST00000360319.8:c.7125T>G	ENSP00000353467.4:p.Ile2375Met
ENST00000369850.7:c.7149T>G	ENSP00000358866.3:p.Ile2383Met
ENST00000369856.7:c.7068T>G	ENSP00000358872.4:p.Ile2356Met
ENST00000420627.5:c.7105T>G	ENSP00000408921.1:n.7105T>G
ENST00000422373.5:c.7125T>G	ENSP00000416926.1:p.Ile2375Met
ENST00000490936.5:n.3677T>G
ENST00000498411.1:n.67+1901T>G
ENST00000498491.5:n.190T>G
ENST00000610817.4:c.6153T>G	ENSP00000480593.1:p.Ile2051Met
NM_001110556.1:c.7149T>G	NP_001104026.1:p.Ile2383Met
NM_001456.3:c.7125T>G	NP_001447.2:p.Ile2375Met
XM_011531127.1:c.7053T>G	XP_011529429.1:p.Ile2351Met
XM_011531128.1:c.7029T>G	XP_011529430.1:p.Ile2343Met
XM_011531129.1:c.6975T>G	XP_011529431.1:p.Ile2325Met
XM_011531130.1:c.6951T>G	XP_011529432.1:p.Ile2317Met
XM_011531131.1:c.6948T>G	XP_011529433.1:p.Ile2316Met
NM_001110556.2:c.7149T>G MANE Select	NP_001104026.1:p.Ile2383Met
NM_001456.4:c.7125T>G	NP_001447.2:p.Ile2375Met