Canonical Allele Identifier: CA519276498

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153579284A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350916A>G , CM000685.2:g.154350916A>G	GRCh38
NC_000023.10:g.153579284A>G , CM000685.1:g.153579284A>G	GRCh37
NC_000023.9:g.153232478A>G	NCBI36
NG_011506.1:g.28723T>C
NG_011506.2:g.28723T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7125T>C	ENSP00000353467.4:p.Ile2375=
ENST00000369850.10:c.7149T>C MANE Select	ENSP00000358866.3:p.Ile2383=
ENST00000369856.8:c.7068T>C	ENSP00000358872.4:p.Ile2356=
ENST00000422373.6:c.3930T>C	ENSP00000416926.2:p.Ile1310=
ENST00000610817.5:c.7206T>C	ENSP00000480593.2:n.7206T>C
ENST00000673639.2:c.280-2226T>C
ENST00000676696.1:c.7428T>C	ENSP00000503392.1:n.7428T>C
ENST00000678304.1:n.2867T>C
ENST00000344736.8:c.7029T>C	ENSP00000358863.3:p.Ile2343=
ENST00000360319.8:c.7125T>C	ENSP00000353467.4:p.Ile2375=
ENST00000369850.7:c.7149T>C	ENSP00000358866.3:p.Ile2383=
ENST00000369856.7:c.7068T>C	ENSP00000358872.4:p.Ile2356=
ENST00000420627.5:c.7105T>C	ENSP00000408921.1:n.7105T>C
ENST00000422373.5:c.7125T>C	ENSP00000416926.1:p.Ile2375=
ENST00000490936.5:n.3677T>C
ENST00000498411.1:n.67+1901T>C
ENST00000498491.5:n.190T>C
ENST00000610817.4:c.6153T>C	ENSP00000480593.1:p.Ile2051=
NM_001110556.1:c.7149T>C	NP_001104026.1:p.Ile2383=
NM_001456.3:c.7125T>C	NP_001447.2:p.Ile2375=
XM_011531127.1:c.7053T>C	XP_011529429.1:p.Ile2351=
XM_011531128.1:c.7029T>C	XP_011529430.1:p.Ile2343=
XM_011531129.1:c.6975T>C	XP_011529431.1:p.Ile2325=
XM_011531130.1:c.6951T>C	XP_011529432.1:p.Ile2317=
XM_011531131.1:c.6948T>C	XP_011529433.1:p.Ile2316=
NM_001110556.2:c.7149T>C MANE Select	NP_001104026.1:p.Ile2383=
NM_001456.4:c.7125T>C	NP_001447.2:p.Ile2375=