Canonical Allele Identifier: CA519706118

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581258G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352890G>T , CM000685.2:g.154352890G>T	GRCh38
NC_000023.10:g.153581258G>T , CM000685.1:g.153581258G>T	GRCh37
NC_000023.9:g.153234452G>T	NCBI36
NG_011506.1:g.26749C>A
NG_011506.2:g.26749C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6237C>A	ENSP00000353467.4:p.Pro2079=
ENST00000369850.10:c.6261C>A MANE Select	ENSP00000358866.3:p.Pro2087=
ENST00000369856.8:c.6180C>A	ENSP00000358872.4:p.Pro2060=
ENST00000422373.6:c.3161-215C>A	ENSP00000416926.2:n.3161-215C>A
ENST00000610817.5:c.6318C>A	ENSP00000480593.2:n.6318C>A
ENST00000673639.2:c.280-4200C>A
ENST00000676696.1:c.6540C>A	ENSP00000503392.1:n.6540C>A
ENST00000678304.1:n.1440C>A
ENST00000344736.8:c.6141C>A	ENSP00000358863.3:p.Pro2047=
ENST00000360319.8:c.6237C>A	ENSP00000353467.4:p.Pro2079=
ENST00000369850.7:c.6261C>A	ENSP00000358866.3:p.Pro2087=
ENST00000369856.7:c.6180C>A	ENSP00000358872.4:p.Pro2060=
ENST00000415241.1:c.463C>A
ENST00000420627.5:c.6217C>A	ENSP00000408921.1:n.6217C>A
ENST00000422373.5:c.6237C>A	ENSP00000416926.1:p.Pro2079=
ENST00000444578.1:c.204C>A	ENSP00000397824.1:p.Pro68=
ENST00000466325.1:n.476C>A
ENST00000490936.5:n.2250C>A
ENST00000610817.4:c.5844+503C>A	ENSP00000480593.1:n.5844+503C>A
NM_001110556.1:c.6261C>A	NP_001104026.1:p.Pro2087=
NM_001456.3:c.6237C>A	NP_001447.2:p.Pro2079=
XM_011531127.1:c.6165C>A	XP_011529429.1:p.Pro2055=
XM_011531128.1:c.6141C>A	XP_011529430.1:p.Pro2047=
XM_011531129.1:c.6087C>A	XP_011529431.1:p.Pro2029=
XM_011531130.1:c.6063C>A	XP_011529432.1:p.Pro2021=
XM_011531131.1:c.6060C>A	XP_011529433.1:p.Pro2020=
NM_001110556.2:c.6261C>A MANE Select	NP_001104026.1:p.Pro2087=
NM_001456.4:c.6237C>A	NP_001447.2:p.Pro2079=