Canonical Allele Identifier: CA519706799

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581568A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353200A>T , CM000685.2:g.154353200A>T	GRCh38
NC_000023.10:g.153581568A>T , CM000685.1:g.153581568A>T	GRCh37
NC_000023.9:g.153234762A>T	NCBI36
NG_011506.1:g.26439T>A
NG_011506.2:g.26439T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6003T>A	ENSP00000353467.4:p.Ile2001=
ENST00000369850.10:c.6027T>A MANE Select	ENSP00000358866.3:p.Ile2009=
ENST00000369856.8:c.5946T>A	ENSP00000358872.4:p.Ile1982=
ENST00000422373.6:c.3161-525T>A	ENSP00000416926.2:n.3161-525T>A
ENST00000610817.5:c.6084T>A	ENSP00000480593.2:n.6084T>A
ENST00000673639.2:c.280-4510T>A
ENST00000676696.1:c.6306T>A	ENSP00000503392.1:n.6306T>A
ENST00000678304.1:n.1206T>A
ENST00000344736.8:c.5907T>A	ENSP00000358863.3:p.Ile1969=
ENST00000360319.8:c.6003T>A	ENSP00000353467.4:p.Ile2001=
ENST00000369850.7:c.6027T>A	ENSP00000358866.3:p.Ile2009=
ENST00000369856.7:c.5946T>A	ENSP00000358872.4:p.Ile1982=
ENST00000415241.1:c.229T>A
ENST00000420627.5:c.5983T>A	ENSP00000408921.1:n.5983T>A
ENST00000422373.5:c.6003T>A	ENSP00000416926.1:p.Ile2001=
ENST00000466325.1:n.166T>A
ENST00000490936.5:n.2016T>A
ENST00000610817.4:c.5844+193T>A	ENSP00000480593.1:n.5844+193T>A
NM_001110556.1:c.6027T>A	NP_001104026.1:p.Ile2009=
NM_001456.3:c.6003T>A	NP_001447.2:p.Ile2001=
XM_011531127.1:c.5931T>A	XP_011529429.1:p.Ile1977=
XM_011531128.1:c.5907T>A	XP_011529430.1:p.Ile1969=
XM_011531129.1:c.5853T>A	XP_011529431.1:p.Ile1951=
XM_011531130.1:c.5829T>A	XP_011529432.1:p.Ile1943=
XM_011531131.1:c.5826T>A	XP_011529433.1:p.Ile1942=
NM_001110556.2:c.6027T>A MANE Select	NP_001104026.1:p.Ile2009=
NM_001456.4:c.6003T>A	NP_001447.2:p.Ile2001=