Canonical Allele Identifier: CA519276500

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153579287T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350919T>C , CM000685.2:g.154350919T>C	GRCh38
NC_000023.10:g.153579287T>C , CM000685.1:g.153579287T>C	GRCh37
NC_000023.9:g.153232481T>C	NCBI36
NG_011506.1:g.28720A>G
NG_011506.2:g.28720A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.7122A>G	ENSP00000353467.4:p.Glu2374=
ENST00000369850.10:c.7146A>G MANE Select	ENSP00000358866.3:p.Glu2382=
ENST00000369856.8:c.7065A>G	ENSP00000358872.4:p.Glu2355=
ENST00000422373.6:c.3927A>G	ENSP00000416926.2:p.Glu1309=
ENST00000610817.5:c.7203A>G	ENSP00000480593.2:n.7203A>G
ENST00000673639.2:c.280-2229A>G
ENST00000676696.1:c.7425A>G	ENSP00000503392.1:n.7425A>G
ENST00000678304.1:n.2864A>G
ENST00000344736.8:c.7026A>G	ENSP00000358863.3:p.Glu2342=
ENST00000360319.8:c.7122A>G	ENSP00000353467.4:p.Glu2374=
ENST00000369850.7:c.7146A>G	ENSP00000358866.3:p.Glu2382=
ENST00000369856.7:c.7065A>G	ENSP00000358872.4:p.Glu2355=
ENST00000420627.5:c.7102A>G	ENSP00000408921.1:n.7102A>G
ENST00000422373.5:c.7122A>G	ENSP00000416926.1:p.Glu2374=
ENST00000490936.5:n.3674A>G
ENST00000498411.1:n.67+1898A>G
ENST00000498491.5:n.187A>G
ENST00000610817.4:c.6150A>G	ENSP00000480593.1:p.Glu2050=
NM_001110556.1:c.7146A>G	NP_001104026.1:p.Glu2382=
NM_001456.3:c.7122A>G	NP_001447.2:p.Glu2374=
XM_011531127.1:c.7050A>G	XP_011529429.1:p.Glu2350=
XM_011531128.1:c.7026A>G	XP_011529430.1:p.Glu2342=
XM_011531129.1:c.6972A>G	XP_011529431.1:p.Glu2324=
XM_011531130.1:c.6948A>G	XP_011529432.1:p.Glu2316=
XM_011531131.1:c.6945A>G	XP_011529433.1:p.Glu2315=
NM_001110556.2:c.7146A>G MANE Select	NP_001104026.1:p.Glu2382=
NM_001456.4:c.7122A>G	NP_001447.2:p.Glu2374=