Canonical Allele Identifier: CA519706198

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581448A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353080A>T , CM000685.2:g.154353080A>T	GRCh38
NC_000023.10:g.153581448A>T , CM000685.1:g.153581448A>T	GRCh37
NC_000023.9:g.153234642A>T	NCBI36
NG_011506.1:g.26559T>A
NG_011506.2:g.26559T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6123T>A	ENSP00000353467.4:p.Arg2041=
ENST00000369850.10:c.6147T>A MANE Select	ENSP00000358866.3:p.Arg2049=
ENST00000369856.8:c.6066T>A	ENSP00000358872.4:p.Arg2022=
ENST00000422373.6:c.3161-405T>A	ENSP00000416926.2:n.3161-405T>A
ENST00000610817.5:c.6204T>A	ENSP00000480593.2:n.6204T>A
ENST00000673639.2:c.280-4390T>A
ENST00000676696.1:c.6426T>A	ENSP00000503392.1:n.6426T>A
ENST00000678304.1:n.1326T>A
ENST00000344736.8:c.6027T>A	ENSP00000358863.3:p.Arg2009=
ENST00000360319.8:c.6123T>A	ENSP00000353467.4:p.Arg2041=
ENST00000369850.7:c.6147T>A	ENSP00000358866.3:p.Arg2049=
ENST00000369856.7:c.6066T>A	ENSP00000358872.4:p.Arg2022=
ENST00000415241.1:c.349T>A
ENST00000420627.5:c.6103T>A	ENSP00000408921.1:n.6103T>A
ENST00000422373.5:c.6123T>A	ENSP00000416926.1:p.Arg2041=
ENST00000444578.1:c.90T>A	ENSP00000397824.1:p.Arg30=
ENST00000466325.1:n.286T>A
ENST00000490936.5:n.2136T>A
ENST00000610817.4:c.5844+313T>A	ENSP00000480593.1:n.5844+313T>A
NM_001110556.1:c.6147T>A	NP_001104026.1:p.Arg2049=
NM_001456.3:c.6123T>A	NP_001447.2:p.Arg2041=
XM_011531127.1:c.6051T>A	XP_011529429.1:p.Arg2017=
XM_011531128.1:c.6027T>A	XP_011529430.1:p.Arg2009=
XM_011531129.1:c.5973T>A	XP_011529431.1:p.Arg1991=
XM_011531130.1:c.5949T>A	XP_011529432.1:p.Arg1983=
XM_011531131.1:c.5946T>A	XP_011529433.1:p.Arg1982=
NM_001110556.2:c.6147T>A MANE Select	NP_001104026.1:p.Arg2049=
NM_001456.4:c.6123T>A	NP_001447.2:p.Arg2041=