Canonical Allele Identifier: CA415197033

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581679G>C (hg19) ; chrX:g.154353311G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353311G>C , CM000685.2:g.154353311G>C	GRCh38
NC_000023.10:g.153581679G>C , CM000685.1:g.153581679G>C	GRCh37
NC_000023.9:g.153234873G>C	NCBI36
NG_011506.1:g.26328C>G
NG_011506.2:g.26328C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5983C>G	ENSP00000353467.4:p.Arg1995Gly
ENST00000369850.10:c.6007C>G MANE Select	ENSP00000358866.3:p.Arg2003Gly
ENST00000369856.8:c.5926C>G	ENSP00000358872.4:p.Arg1976Gly
ENST00000422373.6:c.3161-636C>G	ENSP00000416926.2:n.3161-636C>G
ENST00000610817.5:c.6064C>G	ENSP00000480593.2:n.6064C>G
ENST00000673639.2:c.280-4621C>G
ENST00000676696.1:c.6286C>G	ENSP00000503392.1:n.6286C>G
ENST00000678304.1:n.1186C>G
ENST00000344736.8:c.5887C>G	ENSP00000358863.3:p.Arg1963Gly
ENST00000360319.8:c.5983C>G	ENSP00000353467.4:p.Arg1995Gly
ENST00000369850.7:c.6007C>G	ENSP00000358866.3:p.Arg2003Gly
ENST00000369856.7:c.5926C>G	ENSP00000358872.4:p.Arg1976Gly
ENST00000415241.1:c.192C>G
ENST00000420627.5:c.5963C>G	ENSP00000408921.1:n.5963C>G
ENST00000422373.5:c.5983C>G	ENSP00000416926.1:p.Arg1995Gly
ENST00000438732.2:c.681C>G
ENST00000466325.1:n.146C>G
ENST00000490936.5:n.1996C>G
ENST00000610817.4:c.5844+82C>G	ENSP00000480593.1:n.5844+82C>G
NM_001110556.1:c.6007C>G	NP_001104026.1:p.Arg2003Gly
NM_001456.3:c.5983C>G	NP_001447.2:p.Arg1995Gly
XM_011531127.1:c.5911C>G	XP_011529429.1:p.Arg1971Gly
XM_011531128.1:c.5887C>G	XP_011529430.1:p.Arg1963Gly
XM_011531129.1:c.5833C>G	XP_011529431.1:p.Arg1945Gly
XM_011531130.1:c.5809C>G	XP_011529432.1:p.Arg1937Gly
XM_011531131.1:c.5806C>G	XP_011529433.1:p.Arg1936Gly
NM_001110556.2:c.6007C>G MANE Select	NP_001104026.1:p.Arg2003Gly
NM_001456.4:c.5983C>G	NP_001447.2:p.Arg1995Gly