Canonical Allele Identifier: CA519706637

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581502G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353134G>T , CM000685.2:g.154353134G>T	GRCh38
NC_000023.10:g.153581502G>T , CM000685.1:g.153581502G>T	GRCh37
NC_000023.9:g.153234696G>T	NCBI36
NG_011506.1:g.26505C>A
NG_011506.2:g.26505C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6069C>A	ENSP00000353467.4:p.Ala2023=
ENST00000369850.10:c.6093C>A MANE Select	ENSP00000358866.3:p.Ala2031=
ENST00000369856.8:c.6012C>A	ENSP00000358872.4:p.Ala2004=
ENST00000422373.6:c.3161-459C>A	ENSP00000416926.2:n.3161-459C>A
ENST00000610817.5:c.6150C>A	ENSP00000480593.2:n.6150C>A
ENST00000673639.2:c.280-4444C>A
ENST00000676696.1:c.6372C>A	ENSP00000503392.1:n.6372C>A
ENST00000678304.1:n.1272C>A
ENST00000344736.8:c.5973C>A	ENSP00000358863.3:p.Ala1991=
ENST00000360319.8:c.6069C>A	ENSP00000353467.4:p.Ala2023=
ENST00000369850.7:c.6093C>A	ENSP00000358866.3:p.Ala2031=
ENST00000369856.7:c.6012C>A	ENSP00000358872.4:p.Ala2004=
ENST00000415241.1:c.295C>A
ENST00000420627.5:c.6049C>A	ENSP00000408921.1:n.6049C>A
ENST00000422373.5:c.6069C>A	ENSP00000416926.1:p.Ala2023=
ENST00000444578.1:c.36C>A	ENSP00000397824.1:p.Ala12=
ENST00000466325.1:n.232C>A
ENST00000490936.5:n.2082C>A
ENST00000610817.4:c.5844+259C>A	ENSP00000480593.1:n.5844+259C>A
NM_001110556.1:c.6093C>A	NP_001104026.1:p.Ala2031=
NM_001456.3:c.6069C>A	NP_001447.2:p.Ala2023=
XM_011531127.1:c.5997C>A	XP_011529429.1:p.Ala1999=
XM_011531128.1:c.5973C>A	XP_011529430.1:p.Ala1991=
XM_011531129.1:c.5919C>A	XP_011529431.1:p.Ala1973=
XM_011531130.1:c.5895C>A	XP_011529432.1:p.Ala1965=
XM_011531131.1:c.5892C>A	XP_011529433.1:p.Ala1964=
NM_001110556.2:c.6093C>A MANE Select	NP_001104026.1:p.Ala2031=
NM_001456.4:c.6069C>A	NP_001447.2:p.Ala2023=