Canonical Allele Identifier: CA415185168

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153579365G>T (hg19) ; chrX:g.154350997G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350997G>T , CM000685.2:g.154350997G>T	GRCh38
NC_000023.10:g.153579365G>T , CM000685.1:g.153579365G>T	GRCh37
NC_000023.9:g.153232559G>T	NCBI36
NG_011506.1:g.28642C>A
NG_011506.2:g.28642C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7044C>A	ENSP00000353467.4:p.Ser2348Arg
ENST00000369850.10:c.7068C>A MANE Select	ENSP00000358866.3:p.Ser2356Arg
ENST00000369856.8:c.6987C>A	ENSP00000358872.4:p.Ser2329Arg
ENST00000422373.6:c.3849C>A	ENSP00000416926.2:p.Ser1283Arg
ENST00000610817.5:c.7125C>A	ENSP00000480593.2:n.7125C>A
ENST00000673639.2:c.280-2307C>A
ENST00000676696.1:c.7347C>A	ENSP00000503392.1:n.7347C>A
ENST00000678304.1:n.2786C>A
ENST00000344736.8:c.6948C>A	ENSP00000358863.3:p.Ser2316Arg
ENST00000360319.8:c.7044C>A	ENSP00000353467.4:p.Ser2348Arg
ENST00000369850.7:c.7068C>A	ENSP00000358866.3:p.Ser2356Arg
ENST00000369856.7:c.6987C>A	ENSP00000358872.4:p.Ser2329Arg
ENST00000420627.5:c.7024C>A	ENSP00000408921.1:n.7024C>A
ENST00000422373.5:c.7044C>A	ENSP00000416926.1:p.Ser2348Arg
ENST00000490936.5:n.3596C>A
ENST00000498411.1:n.67+1820C>A
ENST00000498491.5:n.109C>A
ENST00000610817.4:c.6072C>A	ENSP00000480593.1:p.Ser2024Arg
NM_001110556.1:c.7068C>A	NP_001104026.1:p.Ser2356Arg
NM_001456.3:c.7044C>A	NP_001447.2:p.Ser2348Arg
XM_011531127.1:c.6972C>A	XP_011529429.1:p.Ser2324Arg
XM_011531128.1:c.6948C>A	XP_011529430.1:p.Ser2316Arg
XM_011531129.1:c.6894C>A	XP_011529431.1:p.Ser2298Arg
XM_011531130.1:c.6870C>A	XP_011529432.1:p.Ser2290Arg
XM_011531131.1:c.6867C>A	XP_011529433.1:p.Ser2289Arg
NM_001110556.2:c.7068C>A MANE Select	NP_001104026.1:p.Ser2356Arg
NM_001456.4:c.7044C>A	NP_001447.2:p.Ser2348Arg