Canonical Allele Identifier: CA415192725

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581039G>T (hg19) ; chrX:g.154352671G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352671G>T , CM000685.2:g.154352671G>T	GRCh38
NC_000023.10:g.153581039G>T , CM000685.1:g.153581039G>T	GRCh37
NC_000023.9:g.153234233G>T	NCBI36
NG_011506.1:g.26968C>A
NG_011506.2:g.26968C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6360C>A	ENSP00000353467.4:p.Ser2120Arg
ENST00000369850.10:c.6384C>A MANE Select	ENSP00000358866.3:p.Ser2128Arg
ENST00000369856.8:c.6303C>A	ENSP00000358872.4:p.Ser2101Arg
ENST00000422373.6:c.3165C>A	ENSP00000416926.2:p.Ser1055Arg
ENST00000610817.5:c.6441C>A	ENSP00000480593.2:n.6441C>A
ENST00000673639.2:c.280-3981C>A
ENST00000676696.1:c.6663C>A	ENSP00000503392.1:n.6663C>A
ENST00000678304.1:n.1563C>A
ENST00000344736.8:c.6264C>A	ENSP00000358863.3:p.Ser2088Arg
ENST00000360319.8:c.6360C>A	ENSP00000353467.4:p.Ser2120Arg
ENST00000369850.7:c.6384C>A	ENSP00000358866.3:p.Ser2128Arg
ENST00000369856.7:c.6303C>A	ENSP00000358872.4:p.Ser2101Arg
ENST00000415241.1:c.586C>A
ENST00000420627.5:c.6340C>A	ENSP00000408921.1:n.6340C>A
ENST00000422373.5:c.6360C>A	ENSP00000416926.1:p.Ser2120Arg
ENST00000444578.1:c.322+101C>A	ENSP00000397824.1:n.322+101C>A
ENST00000466325.1:n.695C>A
ENST00000474358.5:n.17C>A
ENST00000490936.5:n.2373C>A
ENST00000498411.1:n.67+146C>A
ENST00000610817.4:c.5845-721C>A	ENSP00000480593.1:n.5845-721C>A
NM_001110556.1:c.6384C>A	NP_001104026.1:p.Ser2128Arg
NM_001456.3:c.6360C>A	NP_001447.2:p.Ser2120Arg
XM_011531127.1:c.6288C>A	XP_011529429.1:p.Ser2096Arg
XM_011531128.1:c.6264C>A	XP_011529430.1:p.Ser2088Arg
XM_011531129.1:c.6210C>A	XP_011529431.1:p.Ser2070Arg
XM_011531130.1:c.6186C>A	XP_011529432.1:p.Ser2062Arg
XM_011531131.1:c.6183C>A	XP_011529433.1:p.Ser2061Arg
NM_001110556.2:c.6384C>A MANE Select	NP_001104026.1:p.Ser2128Arg
NM_001456.4:c.6360C>A	NP_001447.2:p.Ser2120Arg