Canonical Allele Identifier: CA519706812

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581192T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352824T>A , CM000685.2:g.154352824T>A	GRCh38
NC_000023.10:g.153581192T>A , CM000685.1:g.153581192T>A	GRCh37
NC_000023.9:g.153234386T>A	NCBI36
NG_011506.1:g.26815A>T
NG_011506.2:g.26815A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6303A>T	ENSP00000353467.4:p.Thr2101=
ENST00000369850.10:c.6327A>T MANE Select	ENSP00000358866.3:p.Thr2109=
ENST00000369856.8:c.6246A>T	ENSP00000358872.4:p.Thr2082=
ENST00000422373.6:c.3161-149A>T	ENSP00000416926.2:n.3161-149A>T
ENST00000610817.5:c.6384A>T	ENSP00000480593.2:n.6384A>T
ENST00000673639.2:c.280-4134A>T
ENST00000676696.1:c.6606A>T	ENSP00000503392.1:n.6606A>T
ENST00000678304.1:n.1506A>T
ENST00000344736.8:c.6207A>T	ENSP00000358863.3:p.Thr2069=
ENST00000360319.8:c.6303A>T	ENSP00000353467.4:p.Thr2101=
ENST00000369850.7:c.6327A>T	ENSP00000358866.3:p.Thr2109=
ENST00000369856.7:c.6246A>T	ENSP00000358872.4:p.Thr2082=
ENST00000415241.1:c.529A>T
ENST00000420627.5:c.6283A>T	ENSP00000408921.1:n.6283A>T
ENST00000422373.5:c.6303A>T	ENSP00000416926.1:p.Thr2101=
ENST00000444578.1:c.270A>T	ENSP00000397824.1:p.Thr90=
ENST00000466325.1:n.542A>T
ENST00000490936.5:n.2316A>T
ENST00000498411.1:n.60A>T
ENST00000610817.4:c.5844+569A>T	ENSP00000480593.1:n.5844+569A>T
NM_001110556.1:c.6327A>T	NP_001104026.1:p.Thr2109=
NM_001456.3:c.6303A>T	NP_001447.2:p.Thr2101=
XM_011531127.1:c.6231A>T	XP_011529429.1:p.Thr2077=
XM_011531128.1:c.6207A>T	XP_011529430.1:p.Thr2069=
XM_011531129.1:c.6153A>T	XP_011529431.1:p.Thr2051=
XM_011531130.1:c.6129A>T	XP_011529432.1:p.Thr2043=
XM_011531131.1:c.6126A>T	XP_011529433.1:p.Thr2042=
NM_001110556.2:c.6327A>T MANE Select	NP_001104026.1:p.Thr2109=
NM_001456.4:c.6303A>T	NP_001447.2:p.Thr2101=