Canonical Allele Identifier: CA415195371

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581407A>T (hg19) ; chrX:g.154353039A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353039A>T , CM000685.2:g.154353039A>T	GRCh38
NC_000023.10:g.153581407A>T , CM000685.1:g.153581407A>T	GRCh37
NC_000023.9:g.153234601A>T	NCBI36
NG_011506.1:g.26600T>A
NG_011506.2:g.26600T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6164T>A	ENSP00000353467.4:p.Phe2055Tyr
ENST00000369850.10:c.6188T>A MANE Select	ENSP00000358866.3:p.Phe2063Tyr
ENST00000369856.8:c.6107T>A	ENSP00000358872.4:p.Phe2036Tyr
ENST00000422373.6:c.3161-364T>A	ENSP00000416926.2:n.3161-364T>A
ENST00000610817.5:c.6245T>A	ENSP00000480593.2:n.6245T>A
ENST00000673639.2:c.280-4349T>A
ENST00000676696.1:c.6467T>A	ENSP00000503392.1:n.6467T>A
ENST00000678304.1:n.1367T>A
ENST00000344736.8:c.6068T>A	ENSP00000358863.3:p.Phe2023Tyr
ENST00000360319.8:c.6164T>A	ENSP00000353467.4:p.Phe2055Tyr
ENST00000369850.7:c.6188T>A	ENSP00000358866.3:p.Phe2063Tyr
ENST00000369856.7:c.6107T>A	ENSP00000358872.4:p.Phe2036Tyr
ENST00000415241.1:c.390T>A
ENST00000420627.5:c.6144T>A	ENSP00000408921.1:n.6144T>A
ENST00000422373.5:c.6164T>A	ENSP00000416926.1:p.Phe2055Tyr
ENST00000444578.1:c.131T>A	ENSP00000397824.1:p.Phe44Tyr
ENST00000466325.1:n.327T>A
ENST00000490936.5:n.2177T>A
ENST00000610817.4:c.5844+354T>A	ENSP00000480593.1:n.5844+354T>A
NM_001110556.1:c.6188T>A	NP_001104026.1:p.Phe2063Tyr
NM_001456.3:c.6164T>A	NP_001447.2:p.Phe2055Tyr
XM_011531127.1:c.6092T>A	XP_011529429.1:p.Phe2031Tyr
XM_011531128.1:c.6068T>A	XP_011529430.1:p.Phe2023Tyr
XM_011531129.1:c.6014T>A	XP_011529431.1:p.Phe2005Tyr
XM_011531130.1:c.5990T>A	XP_011529432.1:p.Phe1997Tyr
XM_011531131.1:c.5987T>A	XP_011529433.1:p.Phe1996Tyr
NM_001110556.2:c.6188T>A MANE Select	NP_001104026.1:p.Phe2063Tyr
NM_001456.4:c.6164T>A	NP_001447.2:p.Phe2055Tyr