Canonical Allele Identifier: CA519706100

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581219C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352851C>A , CM000685.2:g.154352851C>A	GRCh38
NC_000023.10:g.153581219C>A , CM000685.1:g.153581219C>A	GRCh37
NC_000023.9:g.153234413C>A	NCBI36
NG_011506.1:g.26788G>T
NG_011506.2:g.26788G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6276G>T	ENSP00000353467.4:p.Gly2092=
ENST00000369850.10:c.6300G>T MANE Select	ENSP00000358866.3:p.Gly2100=
ENST00000369856.8:c.6219G>T	ENSP00000358872.4:p.Gly2073=
ENST00000422373.6:c.3161-176G>T	ENSP00000416926.2:n.3161-176G>T
ENST00000610817.5:c.6357G>T	ENSP00000480593.2:n.6357G>T
ENST00000673639.2:c.280-4161G>T
ENST00000676696.1:c.6579G>T	ENSP00000503392.1:n.6579G>T
ENST00000678304.1:n.1479G>T
ENST00000344736.8:c.6180G>T	ENSP00000358863.3:p.Gly2060=
ENST00000360319.8:c.6276G>T	ENSP00000353467.4:p.Gly2092=
ENST00000369850.7:c.6300G>T	ENSP00000358866.3:p.Gly2100=
ENST00000369856.7:c.6219G>T	ENSP00000358872.4:p.Gly2073=
ENST00000415241.1:c.502G>T
ENST00000420627.5:c.6256G>T	ENSP00000408921.1:n.6256G>T
ENST00000422373.5:c.6276G>T	ENSP00000416926.1:p.Gly2092=
ENST00000444578.1:c.243G>T	ENSP00000397824.1:p.Gly81=
ENST00000466325.1:n.515G>T
ENST00000490936.5:n.2289G>T
ENST00000498411.1:n.33G>T
ENST00000610817.4:c.5844+542G>T	ENSP00000480593.1:n.5844+542G>T
NM_001110556.1:c.6300G>T	NP_001104026.1:p.Gly2100=
NM_001456.3:c.6276G>T	NP_001447.2:p.Gly2092=
XM_011531127.1:c.6204G>T	XP_011529429.1:p.Gly2068=
XM_011531128.1:c.6180G>T	XP_011529430.1:p.Gly2060=
XM_011531129.1:c.6126G>T	XP_011529431.1:p.Gly2042=
XM_011531130.1:c.6102G>T	XP_011529432.1:p.Gly2034=
XM_011531131.1:c.6099G>T	XP_011529433.1:p.Gly2033=
NM_001110556.2:c.6300G>T MANE Select	NP_001104026.1:p.Gly2100=
NM_001456.4:c.6276G>T	NP_001447.2:p.Gly2092=