Canonical Allele Identifier: CA415195896

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581467T>C (hg19) ; chrX:g.154353099T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353099T>C , CM000685.2:g.154353099T>C	GRCh38
NC_000023.10:g.153581467T>C , CM000685.1:g.153581467T>C	GRCh37
NC_000023.9:g.153234661T>C	NCBI36
NG_011506.1:g.26540A>G
NG_011506.2:g.26540A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6104A>G	ENSP00000353467.4:p.Glu2035Gly
ENST00000369850.10:c.6128A>G MANE Select	ENSP00000358866.3:p.Glu2043Gly
ENST00000369856.8:c.6047A>G	ENSP00000358872.4:p.Glu2016Gly
ENST00000422373.6:c.3161-424A>G	ENSP00000416926.2:n.3161-424A>G
ENST00000610817.5:c.6185A>G	ENSP00000480593.2:n.6185A>G
ENST00000673639.2:c.280-4409A>G
ENST00000676696.1:c.6407A>G	ENSP00000503392.1:n.6407A>G
ENST00000678304.1:n.1307A>G
ENST00000344736.8:c.6008A>G	ENSP00000358863.3:p.Glu2003Gly
ENST00000360319.8:c.6104A>G	ENSP00000353467.4:p.Glu2035Gly
ENST00000369850.7:c.6128A>G	ENSP00000358866.3:p.Glu2043Gly
ENST00000369856.7:c.6047A>G	ENSP00000358872.4:p.Glu2016Gly
ENST00000415241.1:c.330A>G
ENST00000420627.5:c.6084A>G	ENSP00000408921.1:n.6084A>G
ENST00000422373.5:c.6104A>G	ENSP00000416926.1:p.Glu2035Gly
ENST00000444578.1:c.71A>G	ENSP00000397824.1:p.Glu24Gly
ENST00000466325.1:n.267A>G
ENST00000490936.5:n.2117A>G
ENST00000610817.4:c.5844+294A>G	ENSP00000480593.1:n.5844+294A>G
NM_001110556.1:c.6128A>G	NP_001104026.1:p.Glu2043Gly
NM_001456.3:c.6104A>G	NP_001447.2:p.Glu2035Gly
XM_011531127.1:c.6032A>G	XP_011529429.1:p.Glu2011Gly
XM_011531128.1:c.6008A>G	XP_011529430.1:p.Glu2003Gly
XM_011531129.1:c.5954A>G	XP_011529431.1:p.Glu1985Gly
XM_011531130.1:c.5930A>G	XP_011529432.1:p.Glu1977Gly
XM_011531131.1:c.5927A>G	XP_011529433.1:p.Glu1976Gly
NM_001110556.2:c.6128A>G MANE Select	NP_001104026.1:p.Glu2043Gly
NM_001456.4:c.6104A>G	NP_001447.2:p.Glu2035Gly