Canonical Allele Identifier: CA519706794

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581565T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353197T>C , CM000685.2:g.154353197T>C	GRCh38
NC_000023.10:g.153581565T>C , CM000685.1:g.153581565T>C	GRCh37
NC_000023.9:g.153234759T>C	NCBI36
NG_011506.1:g.26442A>G
NG_011506.2:g.26442A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6006A>G	ENSP00000353467.4:p.Ser2002=
ENST00000369850.10:c.6030A>G MANE Select	ENSP00000358866.3:p.Ser2010=
ENST00000369856.8:c.5949A>G	ENSP00000358872.4:p.Ser1983=
ENST00000422373.6:c.3161-522A>G	ENSP00000416926.2:n.3161-522A>G
ENST00000610817.5:c.6087A>G	ENSP00000480593.2:n.6087A>G
ENST00000673639.2:c.280-4507A>G
ENST00000676696.1:c.6309A>G	ENSP00000503392.1:n.6309A>G
ENST00000678304.1:n.1209A>G
ENST00000344736.8:c.5910A>G	ENSP00000358863.3:p.Ser1970=
ENST00000360319.8:c.6006A>G	ENSP00000353467.4:p.Ser2002=
ENST00000369850.7:c.6030A>G	ENSP00000358866.3:p.Ser2010=
ENST00000369856.7:c.5949A>G	ENSP00000358872.4:p.Ser1983=
ENST00000415241.1:c.232A>G
ENST00000420627.5:c.5986A>G	ENSP00000408921.1:n.5986A>G
ENST00000422373.5:c.6006A>G	ENSP00000416926.1:p.Ser2002=
ENST00000466325.1:n.169A>G
ENST00000490936.5:n.2019A>G
ENST00000610817.4:c.5844+196A>G	ENSP00000480593.1:n.5844+196A>G
NM_001110556.1:c.6030A>G	NP_001104026.1:p.Ser2010=
NM_001456.3:c.6006A>G	NP_001447.2:p.Ser2002=
XM_011531127.1:c.5934A>G	XP_011529429.1:p.Ser1978=
XM_011531128.1:c.5910A>G	XP_011529430.1:p.Ser1970=
XM_011531129.1:c.5856A>G	XP_011529431.1:p.Ser1952=
XM_011531130.1:c.5832A>G	XP_011529432.1:p.Ser1944=
XM_011531131.1:c.5829A>G	XP_011529433.1:p.Ser1943=
NM_001110556.2:c.6030A>G MANE Select	NP_001104026.1:p.Ser2010=
NM_001456.4:c.6006A>G	NP_001447.2:p.Ser2002=