Canonical Allele Identifier: CA519276519

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153579317T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350949T>A , CM000685.2:g.154350949T>A	GRCh38
NC_000023.10:g.153579317T>A , CM000685.1:g.153579317T>A	GRCh37
NC_000023.9:g.153232511T>A	NCBI36
NG_011506.1:g.28690A>T
NG_011506.2:g.28690A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7092A>T	ENSP00000353467.4:p.Ser2364=
ENST00000369850.10:c.7116A>T MANE Select	ENSP00000358866.3:p.Ser2372=
ENST00000369856.8:c.7035A>T	ENSP00000358872.4:p.Ser2345=
ENST00000422373.6:c.3897A>T	ENSP00000416926.2:p.Ser1299=
ENST00000610817.5:c.7173A>T	ENSP00000480593.2:n.7173A>T
ENST00000673639.2:c.280-2259A>T
ENST00000676696.1:c.7395A>T	ENSP00000503392.1:n.7395A>T
ENST00000678304.1:n.2834A>T
ENST00000344736.8:c.6996A>T	ENSP00000358863.3:p.Ser2332=
ENST00000360319.8:c.7092A>T	ENSP00000353467.4:p.Ser2364=
ENST00000369850.7:c.7116A>T	ENSP00000358866.3:p.Ser2372=
ENST00000369856.7:c.7035A>T	ENSP00000358872.4:p.Ser2345=
ENST00000420627.5:c.7072A>T	ENSP00000408921.1:n.7072A>T
ENST00000422373.5:c.7092A>T	ENSP00000416926.1:p.Ser2364=
ENST00000490936.5:n.3644A>T
ENST00000498411.1:n.67+1868A>T
ENST00000498491.5:n.157A>T
ENST00000610817.4:c.6120A>T	ENSP00000480593.1:p.Ser2040=
NM_001110556.1:c.7116A>T	NP_001104026.1:p.Ser2372=
NM_001456.3:c.7092A>T	NP_001447.2:p.Ser2364=
XM_011531127.1:c.7020A>T	XP_011529429.1:p.Ser2340=
XM_011531128.1:c.6996A>T	XP_011529430.1:p.Ser2332=
XM_011531129.1:c.6942A>T	XP_011529431.1:p.Ser2314=
XM_011531130.1:c.6918A>T	XP_011529432.1:p.Ser2306=
XM_011531131.1:c.6915A>T	XP_011529433.1:p.Ser2305=
NM_001110556.2:c.7116A>T MANE Select	NP_001104026.1:p.Ser2372=
NM_001456.4:c.7092A>T	NP_001447.2:p.Ser2364=