Canonical Allele Identifier: CA415197270

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581702T>G (hg19) ; chrX:g.154353334T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353334T>G , CM000685.2:g.154353334T>G	GRCh38
NC_000023.10:g.153581702T>G , CM000685.1:g.153581702T>G	GRCh37
NC_000023.9:g.153234896T>G	NCBI36
NG_011506.1:g.26305A>C
NG_011506.2:g.26305A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5960A>C	ENSP00000353467.4:p.Glu1987Ala
ENST00000369850.10:c.5984A>C MANE Select	ENSP00000358866.3:p.Glu1995Ala
ENST00000369856.8:c.5903A>C	ENSP00000358872.4:p.Glu1968Ala
ENST00000422373.6:c.3161-659A>C	ENSP00000416926.2:n.3161-659A>C
ENST00000610817.5:c.6041A>C	ENSP00000480593.2:n.6041A>C
ENST00000673639.2:c.280-4644A>C
ENST00000676696.1:c.6263A>C	ENSP00000503392.1:n.6263A>C
ENST00000678304.1:n.1163A>C
ENST00000344736.8:c.5864A>C	ENSP00000358863.3:p.Glu1955Ala
ENST00000360319.8:c.5960A>C	ENSP00000353467.4:p.Glu1987Ala
ENST00000369850.7:c.5984A>C	ENSP00000358866.3:p.Glu1995Ala
ENST00000369856.7:c.5903A>C	ENSP00000358872.4:p.Glu1968Ala
ENST00000415241.1:c.169A>C
ENST00000420627.5:c.5940A>C	ENSP00000408921.1:n.5940A>C
ENST00000422373.5:c.5960A>C	ENSP00000416926.1:p.Glu1987Ala
ENST00000438732.2:c.658A>C
ENST00000466325.1:n.123A>C
ENST00000490936.5:n.1973A>C
ENST00000610817.4:c.5844+59A>C	ENSP00000480593.1:n.5844+59A>C
NM_001110556.1:c.5984A>C	NP_001104026.1:p.Glu1995Ala
NM_001456.3:c.5960A>C	NP_001447.2:p.Glu1987Ala
XM_011531127.1:c.5888A>C	XP_011529429.1:p.Glu1963Ala
XM_011531128.1:c.5864A>C	XP_011529430.1:p.Glu1955Ala
XM_011531129.1:c.5810A>C	XP_011529431.1:p.Glu1937Ala
XM_011531130.1:c.5786A>C	XP_011529432.1:p.Glu1929Ala
XM_011531131.1:c.5783A>C	XP_011529433.1:p.Glu1928Ala
NM_001110556.2:c.5984A>C MANE Select	NP_001104026.1:p.Glu1995Ala
NM_001456.4:c.5960A>C	NP_001447.2:p.Glu1987Ala