Canonical Allele Identifier: CA519706712

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581535C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353167C>T , CM000685.2:g.154353167C>T	GRCh38
NC_000023.10:g.153581535C>T , CM000685.1:g.153581535C>T	GRCh37
NC_000023.9:g.153234729C>T	NCBI36
NG_011506.1:g.26472G>A
NG_011506.2:g.26472G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6036G>A	ENSP00000353467.4:p.Leu2012=
ENST00000369850.10:c.6060G>A MANE Select	ENSP00000358866.3:p.Leu2020=
ENST00000369856.8:c.5979G>A	ENSP00000358872.4:p.Leu1993=
ENST00000422373.6:c.3161-492G>A	ENSP00000416926.2:n.3161-492G>A
ENST00000610817.5:c.6117G>A	ENSP00000480593.2:n.6117G>A
ENST00000673639.2:c.280-4477G>A
ENST00000676696.1:c.6339G>A	ENSP00000503392.1:n.6339G>A
ENST00000678304.1:n.1239G>A
ENST00000344736.8:c.5940G>A	ENSP00000358863.3:p.Leu1980=
ENST00000360319.8:c.6036G>A	ENSP00000353467.4:p.Leu2012=
ENST00000369850.7:c.6060G>A	ENSP00000358866.3:p.Leu2020=
ENST00000369856.7:c.5979G>A	ENSP00000358872.4:p.Leu1993=
ENST00000415241.1:c.262G>A
ENST00000420627.5:c.6016G>A	ENSP00000408921.1:n.6016G>A
ENST00000422373.5:c.6036G>A	ENSP00000416926.1:p.Leu2012=
ENST00000444578.1:c.3G>A	ENSP00000397824.1:p.Leu1=
ENST00000466325.1:n.199G>A
ENST00000490936.5:n.2049G>A
ENST00000610817.4:c.5844+226G>A	ENSP00000480593.1:n.5844+226G>A
NM_001110556.1:c.6060G>A	NP_001104026.1:p.Leu2020=
NM_001456.3:c.6036G>A	NP_001447.2:p.Leu2012=
XM_011531127.1:c.5964G>A	XP_011529429.1:p.Leu1988=
XM_011531128.1:c.5940G>A	XP_011529430.1:p.Leu1980=
XM_011531129.1:c.5886G>A	XP_011529431.1:p.Leu1962=
XM_011531130.1:c.5862G>A	XP_011529432.1:p.Leu1954=
XM_011531131.1:c.5859G>A	XP_011529433.1:p.Leu1953=
NM_001110556.2:c.6060G>A MANE Select	NP_001104026.1:p.Leu2020=
NM_001456.4:c.6036G>A	NP_001447.2:p.Leu2012=