Canonical Allele Identifier: CA519706887

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581695A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353327A>G , CM000685.2:g.154353327A>G	GRCh38
NC_000023.10:g.153581695A>G , CM000685.1:g.153581695A>G	GRCh37
NC_000023.9:g.153234889A>G	NCBI36
NG_011506.1:g.26312T>C
NG_011506.2:g.26312T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5967T>C	ENSP00000353467.4:p.Cys1989=
ENST00000369850.10:c.5991T>C MANE Select	ENSP00000358866.3:p.Cys1997=
ENST00000369856.8:c.5910T>C	ENSP00000358872.4:p.Cys1970=
ENST00000422373.6:c.3161-652T>C	ENSP00000416926.2:n.3161-652T>C
ENST00000610817.5:c.6048T>C	ENSP00000480593.2:n.6048T>C
ENST00000673639.2:c.280-4637T>C
ENST00000676696.1:c.6270T>C	ENSP00000503392.1:n.6270T>C
ENST00000678304.1:n.1170T>C
ENST00000344736.8:c.5871T>C	ENSP00000358863.3:p.Cys1957=
ENST00000360319.8:c.5967T>C	ENSP00000353467.4:p.Cys1989=
ENST00000369850.7:c.5991T>C	ENSP00000358866.3:p.Cys1997=
ENST00000369856.7:c.5910T>C	ENSP00000358872.4:p.Cys1970=
ENST00000415241.1:c.176T>C
ENST00000420627.5:c.5947T>C	ENSP00000408921.1:n.5947T>C
ENST00000422373.5:c.5967T>C	ENSP00000416926.1:p.Cys1989=
ENST00000438732.2:c.665T>C
ENST00000466325.1:n.130T>C
ENST00000490936.5:n.1980T>C
ENST00000610817.4:c.5844+66T>C	ENSP00000480593.1:n.5844+66T>C
NM_001110556.1:c.5991T>C	NP_001104026.1:p.Cys1997=
NM_001456.3:c.5967T>C	NP_001447.2:p.Cys1989=
XM_011531127.1:c.5895T>C	XP_011529429.1:p.Cys1965=
XM_011531128.1:c.5871T>C	XP_011529430.1:p.Cys1957=
XM_011531129.1:c.5817T>C	XP_011529431.1:p.Cys1939=
XM_011531130.1:c.5793T>C	XP_011529432.1:p.Cys1931=
XM_011531131.1:c.5790T>C	XP_011529433.1:p.Cys1930=
NM_001110556.2:c.5991T>C MANE Select	NP_001104026.1:p.Cys1997=
NM_001456.4:c.5967T>C	NP_001447.2:p.Cys1989=