Canonical Allele Identifier: CA519706657

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581141A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352773A>G , CM000685.2:g.154352773A>G	GRCh38
NC_000023.10:g.153581141A>G , CM000685.1:g.153581141A>G	GRCh37
NC_000023.9:g.153234335A>G	NCBI36
NG_011506.1:g.26866T>C
NG_011506.2:g.26866T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6354T>C	ENSP00000353467.4:p.Pro2118=
ENST00000369850.10:c.6378T>C MANE Select	ENSP00000358866.3:p.Pro2126=
ENST00000369856.8:c.6297T>C	ENSP00000358872.4:p.Pro2099=
ENST00000422373.6:c.3161-98T>C	ENSP00000416926.2:n.3161-98T>C
ENST00000610817.5:c.6435T>C	ENSP00000480593.2:n.6435T>C
ENST00000673639.2:c.280-4083T>C
ENST00000676696.1:c.6657T>C	ENSP00000503392.1:n.6657T>C
ENST00000678304.1:n.1557T>C
ENST00000344736.8:c.6258T>C	ENSP00000358863.3:p.Pro2086=
ENST00000360319.8:c.6354T>C	ENSP00000353467.4:p.Pro2118=
ENST00000369850.7:c.6378T>C	ENSP00000358866.3:p.Pro2126=
ENST00000369856.7:c.6297T>C	ENSP00000358872.4:p.Pro2099=
ENST00000415241.1:c.580T>C
ENST00000420627.5:c.6334T>C	ENSP00000408921.1:n.6334T>C
ENST00000422373.5:c.6354T>C	ENSP00000416926.1:p.Pro2118=
ENST00000444578.1:c.321T>C	ENSP00000397824.1:p.Pro107=
ENST00000466325.1:n.593T>C
ENST00000474358.5:n.11T>C
ENST00000490936.5:n.2367T>C
ENST00000498411.1:n.67+44T>C
ENST00000610817.4:c.5844+620T>C	ENSP00000480593.1:n.5844+620T>C
NM_001110556.1:c.6378T>C	NP_001104026.1:p.Pro2126=
NM_001456.3:c.6354T>C	NP_001447.2:p.Pro2118=
XM_011531127.1:c.6282T>C	XP_011529429.1:p.Pro2094=
XM_011531128.1:c.6258T>C	XP_011529430.1:p.Pro2086=
XM_011531129.1:c.6204T>C	XP_011529431.1:p.Pro2068=
XM_011531130.1:c.6180T>C	XP_011529432.1:p.Pro2060=
XM_011531131.1:c.6177T>C	XP_011529433.1:p.Pro2059=
NM_001110556.2:c.6378T>C MANE Select	NP_001104026.1:p.Pro2126=
NM_001456.4:c.6354T>C	NP_001447.2:p.Pro2118=