Canonical Allele Identifier: CA415197375

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581714G>T (hg19) ; chrX:g.154353346G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353346G>T , CM000685.2:g.154353346G>T	GRCh38
NC_000023.10:g.153581714G>T , CM000685.1:g.153581714G>T	GRCh37
NC_000023.9:g.153234908G>T	NCBI36
NG_011506.1:g.26293C>A
NG_011506.2:g.26293C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5948C>A	ENSP00000353467.4:p.Ser1983Ter
ENST00000369850.10:c.5972C>A MANE Select	ENSP00000358866.3:p.Ser1991Ter
ENST00000369856.8:c.5891C>A	ENSP00000358872.4:p.Ser1964Ter
ENST00000422373.6:c.3161-671C>A	ENSP00000416926.2:n.3161-671C>A
ENST00000610817.5:c.6029C>A	ENSP00000480593.2:n.6029C>A
ENST00000673639.2:c.280-4656C>A
ENST00000676696.1:c.6251C>A	ENSP00000503392.1:n.6251C>A
ENST00000678304.1:n.1151C>A
ENST00000344736.8:c.5852C>A	ENSP00000358863.3:p.Ser1951Ter
ENST00000360319.8:c.5948C>A	ENSP00000353467.4:p.Ser1983Ter
ENST00000369850.7:c.5972C>A	ENSP00000358866.3:p.Ser1991Ter
ENST00000369856.7:c.5891C>A	ENSP00000358872.4:p.Ser1964Ter
ENST00000415241.1:c.157C>A
ENST00000420627.5:c.5928C>A	ENSP00000408921.1:n.5928C>A
ENST00000422373.5:c.5948C>A	ENSP00000416926.1:p.Ser1983Ter
ENST00000438732.2:c.646C>A
ENST00000466325.1:n.111C>A
ENST00000490936.5:n.1961C>A
ENST00000610817.4:c.5844+47C>A	ENSP00000480593.1:n.5844+47C>A
NM_001110556.1:c.5972C>A	NP_001104026.1:p.Ser1991Ter
NM_001456.3:c.5948C>A	NP_001447.2:p.Ser1983Ter
XM_011531127.1:c.5876C>A	XP_011529429.1:p.Ser1959Ter
XM_011531128.1:c.5852C>A	XP_011529430.1:p.Ser1951Ter
XM_011531129.1:c.5798C>A	XP_011529431.1:p.Ser1933Ter
XM_011531130.1:c.5774C>A	XP_011529432.1:p.Ser1925Ter
XM_011531131.1:c.5771C>A	XP_011529433.1:p.Ser1924Ter
NM_001110556.2:c.5972C>A MANE Select	NP_001104026.1:p.Ser1991Ter
NM_001456.4:c.5948C>A	NP_001447.2:p.Ser1983Ter