Canonical Allele Identifier: CA519706705

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581156G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352788G>T , CM000685.2:g.154352788G>T	GRCh38
NC_000023.10:g.153581156G>T , CM000685.1:g.153581156G>T	GRCh37
NC_000023.9:g.153234350G>T	NCBI36
NG_011506.1:g.26851C>A
NG_011506.2:g.26851C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6339C>A	ENSP00000353467.4:p.Ala2113=
ENST00000369850.10:c.6363C>A MANE Select	ENSP00000358866.3:p.Ala2121=
ENST00000369856.8:c.6282C>A	ENSP00000358872.4:p.Ala2094=
ENST00000422373.6:c.3161-113C>A	ENSP00000416926.2:n.3161-113C>A
ENST00000610817.5:c.6420C>A	ENSP00000480593.2:n.6420C>A
ENST00000673639.2:c.280-4098C>A
ENST00000676696.1:c.6642C>A	ENSP00000503392.1:n.6642C>A
ENST00000678304.1:n.1542C>A
ENST00000344736.8:c.6243C>A	ENSP00000358863.3:p.Ala2081=
ENST00000360319.8:c.6339C>A	ENSP00000353467.4:p.Ala2113=
ENST00000369850.7:c.6363C>A	ENSP00000358866.3:p.Ala2121=
ENST00000369856.7:c.6282C>A	ENSP00000358872.4:p.Ala2094=
ENST00000415241.1:c.565C>A
ENST00000420627.5:c.6319C>A	ENSP00000408921.1:n.6319C>A
ENST00000422373.5:c.6339C>A	ENSP00000416926.1:p.Ala2113=
ENST00000444578.1:c.306C>A	ENSP00000397824.1:p.Ala102=
ENST00000466325.1:n.578C>A
ENST00000490936.5:n.2352C>A
ENST00000498411.1:n.67+29C>A
ENST00000610817.4:c.5844+605C>A	ENSP00000480593.1:n.5844+605C>A
NM_001110556.1:c.6363C>A	NP_001104026.1:p.Ala2121=
NM_001456.3:c.6339C>A	NP_001447.2:p.Ala2113=
XM_011531127.1:c.6267C>A	XP_011529429.1:p.Ala2089=
XM_011531128.1:c.6243C>A	XP_011529430.1:p.Ala2081=
XM_011531129.1:c.6189C>A	XP_011529431.1:p.Ala2063=
XM_011531130.1:c.6165C>A	XP_011529432.1:p.Ala2055=
XM_011531131.1:c.6162C>A	XP_011529433.1:p.Ala2054=
NM_001110556.2:c.6363C>A MANE Select	NP_001104026.1:p.Ala2121=
NM_001456.4:c.6339C>A	NP_001447.2:p.Ala2113=