Canonical Allele Identifier: CA519706157

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581391A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353023A>G , CM000685.2:g.154353023A>G	GRCh38
NC_000023.10:g.153581391A>G , CM000685.1:g.153581391A>G	GRCh37
NC_000023.9:g.153234585A>G	NCBI36
NG_011506.1:g.26616T>C
NG_011506.2:g.26616T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6180T>C	ENSP00000353467.4:p.Phe2060=
ENST00000369850.10:c.6204T>C MANE Select	ENSP00000358866.3:p.Phe2068=
ENST00000369856.8:c.6123T>C	ENSP00000358872.4:p.Phe2041=
ENST00000422373.6:c.3161-348T>C	ENSP00000416926.2:n.3161-348T>C
ENST00000610817.5:c.6261T>C	ENSP00000480593.2:n.6261T>C
ENST00000673639.2:c.280-4333T>C
ENST00000676696.1:c.6483T>C	ENSP00000503392.1:n.6483T>C
ENST00000678304.1:n.1383T>C
ENST00000344736.8:c.6084T>C	ENSP00000358863.3:p.Phe2028=
ENST00000360319.8:c.6180T>C	ENSP00000353467.4:p.Phe2060=
ENST00000369850.7:c.6204T>C	ENSP00000358866.3:p.Phe2068=
ENST00000369856.7:c.6123T>C	ENSP00000358872.4:p.Phe2041=
ENST00000415241.1:c.406T>C
ENST00000420627.5:c.6160T>C	ENSP00000408921.1:n.6160T>C
ENST00000422373.5:c.6180T>C	ENSP00000416926.1:p.Phe2060=
ENST00000444578.1:c.147T>C	ENSP00000397824.1:p.Phe49=
ENST00000466325.1:n.343T>C
ENST00000490936.5:n.2193T>C
ENST00000610817.4:c.5844+370T>C	ENSP00000480593.1:n.5844+370T>C
NM_001110556.1:c.6204T>C	NP_001104026.1:p.Phe2068=
NM_001456.3:c.6180T>C	NP_001447.2:p.Phe2060=
XM_011531127.1:c.6108T>C	XP_011529429.1:p.Phe2036=
XM_011531128.1:c.6084T>C	XP_011529430.1:p.Phe2028=
XM_011531129.1:c.6030T>C	XP_011529431.1:p.Phe2010=
XM_011531130.1:c.6006T>C	XP_011529432.1:p.Phe2002=
XM_011531131.1:c.6003T>C	XP_011529433.1:p.Phe2001=
NM_001110556.2:c.6204T>C MANE Select	NP_001104026.1:p.Phe2068=
NM_001456.4:c.6180T>C	NP_001447.2:p.Phe2060=