Canonical Allele Identifier: CA519706202

Gene: FLNA

Linked Data

• dbSNP Id: rs1557176124
• gnomAD v2: X-153581454-G-T
• gnomAD v3: X-154353086-G-T
• gnomAD v4: X-154353086-G-T
• MyVariant Identifiers: chrX:g.153581454G>T (hg19) ; chrX:g.154353086G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353086G>T , CM000685.2:g.154353086G>T	GRCh38
NC_000023.10:g.153581454G>T , CM000685.1:g.153581454G>T	GRCh37
NC_000023.9:g.153234648G>T	NCBI36
NG_011506.1:g.26553C>A
NG_011506.2:g.26553C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6117C>A	ENSP00000353467.4:p.Ala2039=
ENST00000369850.10:c.6141C>A MANE Select	ENSP00000358866.3:p.Ala2047=
ENST00000369856.8:c.6060C>A	ENSP00000358872.4:p.Ala2020=
ENST00000422373.6:c.3161-411C>A	ENSP00000416926.2:n.3161-411C>A
ENST00000610817.5:c.6198C>A	ENSP00000480593.2:n.6198C>A
ENST00000673639.2:c.280-4396C>A
ENST00000676696.1:c.6420C>A	ENSP00000503392.1:n.6420C>A
ENST00000678304.1:n.1320C>A
ENST00000344736.8:c.6021C>A	ENSP00000358863.3:p.Ala2007=
ENST00000360319.8:c.6117C>A	ENSP00000353467.4:p.Ala2039=
ENST00000369850.7:c.6141C>A	ENSP00000358866.3:p.Ala2047=
ENST00000369856.7:c.6060C>A	ENSP00000358872.4:p.Ala2020=
ENST00000415241.1:c.343C>A
ENST00000420627.5:c.6097C>A	ENSP00000408921.1:n.6097C>A
ENST00000422373.5:c.6117C>A	ENSP00000416926.1:p.Ala2039=
ENST00000444578.1:c.84C>A	ENSP00000397824.1:p.Ala28=
ENST00000466325.1:n.280C>A
ENST00000490936.5:n.2130C>A
ENST00000610817.4:c.5844+307C>A	ENSP00000480593.1:n.5844+307C>A
NM_001110556.1:c.6141C>A	NP_001104026.1:p.Ala2047=
NM_001456.3:c.6117C>A	NP_001447.2:p.Ala2039=
XM_011531127.1:c.6045C>A	XP_011529429.1:p.Ala2015=
XM_011531128.1:c.6021C>A	XP_011529430.1:p.Ala2007=
XM_011531129.1:c.5967C>A	XP_011529431.1:p.Ala1989=
XM_011531130.1:c.5943C>A	XP_011529432.1:p.Ala1981=
XM_011531131.1:c.5940C>A	XP_011529433.1:p.Ala1980=
NM_001110556.2:c.6141C>A MANE Select	NP_001104026.1:p.Ala2047=
NM_001456.4:c.6117C>A	NP_001447.2:p.Ala2039=