Canonical Allele Identifier: CA519706161

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581397T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353029T>G , CM000685.2:g.154353029T>G	GRCh38
NC_000023.10:g.153581397T>G , CM000685.1:g.153581397T>G	GRCh37
NC_000023.9:g.153234591T>G	NCBI36
NG_011506.1:g.26610A>C
NG_011506.2:g.26610A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6174A>C	ENSP00000353467.4:p.Ala2058=
ENST00000369850.10:c.6198A>C MANE Select	ENSP00000358866.3:p.Ala2066=
ENST00000369856.8:c.6117A>C	ENSP00000358872.4:p.Ala2039=
ENST00000422373.6:c.3161-354A>C	ENSP00000416926.2:n.3161-354A>C
ENST00000610817.5:c.6255A>C	ENSP00000480593.2:n.6255A>C
ENST00000673639.2:c.280-4339A>C
ENST00000676696.1:c.6477A>C	ENSP00000503392.1:n.6477A>C
ENST00000678304.1:n.1377A>C
ENST00000344736.8:c.6078A>C	ENSP00000358863.3:p.Ala2026=
ENST00000360319.8:c.6174A>C	ENSP00000353467.4:p.Ala2058=
ENST00000369850.7:c.6198A>C	ENSP00000358866.3:p.Ala2066=
ENST00000369856.7:c.6117A>C	ENSP00000358872.4:p.Ala2039=
ENST00000415241.1:c.400A>C
ENST00000420627.5:c.6154A>C	ENSP00000408921.1:n.6154A>C
ENST00000422373.5:c.6174A>C	ENSP00000416926.1:p.Ala2058=
ENST00000444578.1:c.141A>C	ENSP00000397824.1:p.Ala47=
ENST00000466325.1:n.337A>C
ENST00000490936.5:n.2187A>C
ENST00000610817.4:c.5844+364A>C	ENSP00000480593.1:n.5844+364A>C
NM_001110556.1:c.6198A>C	NP_001104026.1:p.Ala2066=
NM_001456.3:c.6174A>C	NP_001447.2:p.Ala2058=
XM_011531127.1:c.6102A>C	XP_011529429.1:p.Ala2034=
XM_011531128.1:c.6078A>C	XP_011529430.1:p.Ala2026=
XM_011531129.1:c.6024A>C	XP_011529431.1:p.Ala2008=
XM_011531130.1:c.6000A>C	XP_011529432.1:p.Ala2000=
XM_011531131.1:c.5997A>C	XP_011529433.1:p.Ala1999=
NM_001110556.2:c.6198A>C MANE Select	NP_001104026.1:p.Ala2066=
NM_001456.4:c.6174A>C	NP_001447.2:p.Ala2058=