Canonical Allele Identifier: CA415194523

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581271G>A (hg19) ; chrX:g.154352903G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352903G>A , CM000685.2:g.154352903G>A	GRCh38
NC_000023.10:g.153581271G>A , CM000685.1:g.153581271G>A	GRCh37
NC_000023.9:g.153234465G>A	NCBI36
NG_011506.1:g.26736C>T
NG_011506.2:g.26736C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6224C>T	ENSP00000353467.4:p.Ser2075Phe
ENST00000369850.10:c.6248C>T MANE Select	ENSP00000358866.3:p.Ser2083Phe
ENST00000369856.8:c.6167C>T	ENSP00000358872.4:p.Ser2056Phe
ENST00000422373.6:c.3161-228C>T	ENSP00000416926.2:n.3161-228C>T
ENST00000610817.5:c.6305C>T	ENSP00000480593.2:n.6305C>T
ENST00000673639.2:c.280-4213C>T
ENST00000676696.1:c.6527C>T	ENSP00000503392.1:n.6527C>T
ENST00000678304.1:n.1427C>T
ENST00000344736.8:c.6128C>T	ENSP00000358863.3:p.Ser2043Phe
ENST00000360319.8:c.6224C>T	ENSP00000353467.4:p.Ser2075Phe
ENST00000369850.7:c.6248C>T	ENSP00000358866.3:p.Ser2083Phe
ENST00000369856.7:c.6167C>T	ENSP00000358872.4:p.Ser2056Phe
ENST00000415241.1:c.450C>T
ENST00000420627.5:c.6204C>T	ENSP00000408921.1:n.6204C>T
ENST00000422373.5:c.6224C>T	ENSP00000416926.1:p.Ser2075Phe
ENST00000444578.1:c.191C>T	ENSP00000397824.1:p.Ser64Phe
ENST00000466325.1:n.463C>T
ENST00000490936.5:n.2237C>T
ENST00000610817.4:c.5844+490C>T	ENSP00000480593.1:n.5844+490C>T
NM_001110556.1:c.6248C>T	NP_001104026.1:p.Ser2083Phe
NM_001456.3:c.6224C>T	NP_001447.2:p.Ser2075Phe
XM_011531127.1:c.6152C>T	XP_011529429.1:p.Ser2051Phe
XM_011531128.1:c.6128C>T	XP_011529430.1:p.Ser2043Phe
XM_011531129.1:c.6074C>T	XP_011529431.1:p.Ser2025Phe
XM_011531130.1:c.6050C>T	XP_011529432.1:p.Ser2017Phe
XM_011531131.1:c.6047C>T	XP_011529433.1:p.Ser2016Phe
NM_001110556.2:c.6248C>T MANE Select	NP_001104026.1:p.Ser2083Phe
NM_001456.4:c.6224C>T	NP_001447.2:p.Ser2075Phe