Canonical Allele Identifier: CA519706654

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581511C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353143C>T , CM000685.2:g.154353143C>T	GRCh38
NC_000023.10:g.153581511C>T , CM000685.1:g.153581511C>T	GRCh37
NC_000023.9:g.153234705C>T	NCBI36
NG_011506.1:g.26496G>A
NG_011506.2:g.26496G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6060G>A	ENSP00000353467.4:p.Gln2020=
ENST00000369850.10:c.6084G>A MANE Select	ENSP00000358866.3:p.Gln2028=
ENST00000369856.8:c.6003G>A	ENSP00000358872.4:p.Gln2001=
ENST00000422373.6:c.3161-468G>A	ENSP00000416926.2:n.3161-468G>A
ENST00000610817.5:c.6141G>A	ENSP00000480593.2:n.6141G>A
ENST00000673639.2:c.280-4453G>A
ENST00000676696.1:c.6363G>A	ENSP00000503392.1:n.6363G>A
ENST00000678304.1:n.1263G>A
ENST00000344736.8:c.5964G>A	ENSP00000358863.3:p.Gln1988=
ENST00000360319.8:c.6060G>A	ENSP00000353467.4:p.Gln2020=
ENST00000369850.7:c.6084G>A	ENSP00000358866.3:p.Gln2028=
ENST00000369856.7:c.6003G>A	ENSP00000358872.4:p.Gln2001=
ENST00000415241.1:c.286G>A
ENST00000420627.5:c.6040G>A	ENSP00000408921.1:n.6040G>A
ENST00000422373.5:c.6060G>A	ENSP00000416926.1:p.Gln2020=
ENST00000444578.1:c.27G>A	ENSP00000397824.1:p.Gln9=
ENST00000466325.1:n.223G>A
ENST00000490936.5:n.2073G>A
ENST00000610817.4:c.5844+250G>A	ENSP00000480593.1:n.5844+250G>A
NM_001110556.1:c.6084G>A	NP_001104026.1:p.Gln2028=
NM_001456.3:c.6060G>A	NP_001447.2:p.Gln2020=
XM_011531127.1:c.5988G>A	XP_011529429.1:p.Gln1996=
XM_011531128.1:c.5964G>A	XP_011529430.1:p.Gln1988=
XM_011531129.1:c.5910G>A	XP_011529431.1:p.Gln1970=
XM_011531130.1:c.5886G>A	XP_011529432.1:p.Gln1962=
XM_011531131.1:c.5883G>A	XP_011529433.1:p.Gln1961=
NM_001110556.2:c.6084G>A MANE Select	NP_001104026.1:p.Gln2028=
NM_001456.4:c.6060G>A	NP_001447.2:p.Gln2020=