Canonical Allele Identifier: CA519706155

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581388G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353020G>A , CM000685.2:g.154353020G>A	GRCh38
NC_000023.10:g.153581388G>A , CM000685.1:g.153581388G>A	GRCh37
NC_000023.9:g.153234582G>A	NCBI36
NG_011506.1:g.26619C>T
NG_011506.2:g.26619C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6183C>T	ENSP00000353467.4:p.Ile2061=
ENST00000369850.10:c.6207C>T MANE Select	ENSP00000358866.3:p.Ile2069=
ENST00000369856.8:c.6126C>T	ENSP00000358872.4:p.Ile2042=
ENST00000422373.6:c.3161-345C>T	ENSP00000416926.2:n.3161-345C>T
ENST00000610817.5:c.6264C>T	ENSP00000480593.2:n.6264C>T
ENST00000673639.2:c.280-4330C>T
ENST00000676696.1:c.6486C>T	ENSP00000503392.1:n.6486C>T
ENST00000678304.1:n.1386C>T
ENST00000344736.8:c.6087C>T	ENSP00000358863.3:p.Ile2029=
ENST00000360319.8:c.6183C>T	ENSP00000353467.4:p.Ile2061=
ENST00000369850.7:c.6207C>T	ENSP00000358866.3:p.Ile2069=
ENST00000369856.7:c.6126C>T	ENSP00000358872.4:p.Ile2042=
ENST00000415241.1:c.409C>T
ENST00000420627.5:c.6163C>T	ENSP00000408921.1:n.6163C>T
ENST00000422373.5:c.6183C>T	ENSP00000416926.1:p.Ile2061=
ENST00000444578.1:c.150C>T	ENSP00000397824.1:p.Ile50=
ENST00000466325.1:n.346C>T
ENST00000490936.5:n.2196C>T
ENST00000610817.4:c.5844+373C>T	ENSP00000480593.1:n.5844+373C>T
NM_001110556.1:c.6207C>T	NP_001104026.1:p.Ile2069=
NM_001456.3:c.6183C>T	NP_001447.2:p.Ile2061=
XM_011531127.1:c.6111C>T	XP_011529429.1:p.Ile2037=
XM_011531128.1:c.6087C>T	XP_011529430.1:p.Ile2029=
XM_011531129.1:c.6033C>T	XP_011529431.1:p.Ile2011=
XM_011531130.1:c.6009C>T	XP_011529432.1:p.Ile2003=
XM_011531131.1:c.6006C>T	XP_011529433.1:p.Ile2002=
NM_001110556.2:c.6207C>T MANE Select	NP_001104026.1:p.Ile2069=
NM_001456.4:c.6183C>T	NP_001447.2:p.Ile2061=