Canonical Allele Identifier: CA519706789

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581183G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352815G>C , CM000685.2:g.154352815G>C	GRCh38
NC_000023.10:g.153581183G>C , CM000685.1:g.153581183G>C	GRCh37
NC_000023.9:g.153234377G>C	NCBI36
NG_011506.1:g.26824C>G
NG_011506.2:g.26824C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.6312C>G	ENSP00000353467.4:p.Gly2104=
ENST00000369850.10:c.6336C>G MANE Select	ENSP00000358866.3:p.Gly2112=
ENST00000369856.8:c.6255C>G	ENSP00000358872.4:p.Gly2085=
ENST00000422373.6:c.3161-140C>G	ENSP00000416926.2:n.3161-140C>G
ENST00000610817.5:c.6393C>G	ENSP00000480593.2:n.6393C>G
ENST00000673639.2:c.280-4125C>G
ENST00000676696.1:c.6615C>G	ENSP00000503392.1:n.6615C>G
ENST00000678304.1:n.1515C>G
ENST00000344736.8:c.6216C>G	ENSP00000358863.3:p.Gly2072=
ENST00000360319.8:c.6312C>G	ENSP00000353467.4:p.Gly2104=
ENST00000369850.7:c.6336C>G	ENSP00000358866.3:p.Gly2112=
ENST00000369856.7:c.6255C>G	ENSP00000358872.4:p.Gly2085=
ENST00000415241.1:c.538C>G
ENST00000420627.5:c.6292C>G	ENSP00000408921.1:n.6292C>G
ENST00000422373.5:c.6312C>G	ENSP00000416926.1:p.Gly2104=
ENST00000444578.1:c.279C>G	ENSP00000397824.1:p.Gly93=
ENST00000466325.1:n.551C>G
ENST00000490936.5:n.2325C>G
ENST00000498411.1:n.67+2C>G
ENST00000610817.4:c.5844+578C>G	ENSP00000480593.1:n.5844+578C>G
NM_001110556.1:c.6336C>G	NP_001104026.1:p.Gly2112=
NM_001456.3:c.6312C>G	NP_001447.2:p.Gly2104=
XM_011531127.1:c.6240C>G	XP_011529429.1:p.Gly2080=
XM_011531128.1:c.6216C>G	XP_011529430.1:p.Gly2072=
XM_011531129.1:c.6162C>G	XP_011529431.1:p.Gly2054=
XM_011531130.1:c.6138C>G	XP_011529432.1:p.Gly2046=
XM_011531131.1:c.6135C>G	XP_011529433.1:p.Gly2045=
NM_001110556.2:c.6336C>G MANE Select	NP_001104026.1:p.Gly2112=
NM_001456.4:c.6312C>G	NP_001447.2:p.Gly2104=