Canonical Allele Identifier: CA415194180

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581241T>C (hg19) ; chrX:g.154352873T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352873T>C , CM000685.2:g.154352873T>C	GRCh38
NC_000023.10:g.153581241T>C , CM000685.1:g.153581241T>C	GRCh37
NC_000023.9:g.153234435T>C	NCBI36
NG_011506.1:g.26766A>G
NG_011506.2:g.26766A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6254A>G	ENSP00000353467.4:p.Asn2085Ser
ENST00000369850.10:c.6278A>G MANE Select	ENSP00000358866.3:p.Asn2093Ser
ENST00000369856.8:c.6197A>G	ENSP00000358872.4:p.Asn2066Ser
ENST00000422373.6:c.3161-198A>G	ENSP00000416926.2:n.3161-198A>G
ENST00000610817.5:c.6335A>G	ENSP00000480593.2:n.6335A>G
ENST00000673639.2:c.280-4183A>G
ENST00000676696.1:c.6557A>G	ENSP00000503392.1:n.6557A>G
ENST00000678304.1:n.1457A>G
ENST00000344736.8:c.6158A>G	ENSP00000358863.3:p.Asn2053Ser
ENST00000360319.8:c.6254A>G	ENSP00000353467.4:p.Asn2085Ser
ENST00000369850.7:c.6278A>G	ENSP00000358866.3:p.Asn2093Ser
ENST00000369856.7:c.6197A>G	ENSP00000358872.4:p.Asn2066Ser
ENST00000415241.1:c.480A>G
ENST00000420627.5:c.6234A>G	ENSP00000408921.1:n.6234A>G
ENST00000422373.5:c.6254A>G	ENSP00000416926.1:p.Asn2085Ser
ENST00000444578.1:c.221A>G	ENSP00000397824.1:p.Asn74Ser
ENST00000466325.1:n.493A>G
ENST00000490936.5:n.2267A>G
ENST00000498411.1:n.11A>G
ENST00000610817.4:c.5844+520A>G	ENSP00000480593.1:n.5844+520A>G
NM_001110556.1:c.6278A>G	NP_001104026.1:p.Asn2093Ser
NM_001456.3:c.6254A>G	NP_001447.2:p.Asn2085Ser
XM_011531127.1:c.6182A>G	XP_011529429.1:p.Asn2061Ser
XM_011531128.1:c.6158A>G	XP_011529430.1:p.Asn2053Ser
XM_011531129.1:c.6104A>G	XP_011529431.1:p.Asn2035Ser
XM_011531130.1:c.6080A>G	XP_011529432.1:p.Asn2027Ser
XM_011531131.1:c.6077A>G	XP_011529433.1:p.Asn2026Ser
NM_001110556.2:c.6278A>G MANE Select	NP_001104026.1:p.Asn2093Ser
NM_001456.4:c.6254A>G	NP_001447.2:p.Asn2085Ser