Canonical Allele Identifier: CA519706904

Gene: FLNA

Linked Data

• gnomAD v4: X-154353336-C-T
• MyVariant Identifiers: chrX:g.153581704C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353336C>T , CM000685.2:g.154353336C>T	GRCh38
NC_000023.10:g.153581704C>T , CM000685.1:g.153581704C>T	GRCh37
NC_000023.9:g.153234898C>T	NCBI36
NG_011506.1:g.26303G>A
NG_011506.2:g.26303G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5958G>A	ENSP00000353467.4:p.Glu1986=
ENST00000369850.10:c.5982G>A MANE Select	ENSP00000358866.3:p.Glu1994=
ENST00000369856.8:c.5901G>A	ENSP00000358872.4:p.Glu1967=
ENST00000422373.6:c.3161-661G>A	ENSP00000416926.2:n.3161-661G>A
ENST00000610817.5:c.6039G>A	ENSP00000480593.2:n.6039G>A
ENST00000673639.2:c.280-4646G>A
ENST00000676696.1:c.6261G>A	ENSP00000503392.1:n.6261G>A
ENST00000678304.1:n.1161G>A
ENST00000344736.8:c.5862G>A	ENSP00000358863.3:p.Glu1954=
ENST00000360319.8:c.5958G>A	ENSP00000353467.4:p.Glu1986=
ENST00000369850.7:c.5982G>A	ENSP00000358866.3:p.Glu1994=
ENST00000369856.7:c.5901G>A	ENSP00000358872.4:p.Glu1967=
ENST00000415241.1:c.167G>A
ENST00000420627.5:c.5938G>A	ENSP00000408921.1:n.5938G>A
ENST00000422373.5:c.5958G>A	ENSP00000416926.1:p.Glu1986=
ENST00000438732.2:c.656G>A
ENST00000466325.1:n.121G>A
ENST00000490936.5:n.1971G>A
ENST00000610817.4:c.5844+57G>A	ENSP00000480593.1:n.5844+57G>A
NM_001110556.1:c.5982G>A	NP_001104026.1:p.Glu1994=
NM_001456.3:c.5958G>A	NP_001447.2:p.Glu1986=
XM_011531127.1:c.5886G>A	XP_011529429.1:p.Glu1962=
XM_011531128.1:c.5862G>A	XP_011529430.1:p.Glu1954=
XM_011531129.1:c.5808G>A	XP_011529431.1:p.Glu1936=
XM_011531130.1:c.5784G>A	XP_011529432.1:p.Glu1928=
XM_011531131.1:c.5781G>A	XP_011529433.1:p.Glu1927=
NM_001110556.2:c.5982G>A MANE Select	NP_001104026.1:p.Glu1994=
NM_001456.4:c.5958G>A	NP_001447.2:p.Glu1986=