Canonical Allele Identifier: CA415195039

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581381T>C (hg19) ; chrX:g.154353013T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353013T>C , CM000685.2:g.154353013T>C	GRCh38
NC_000023.10:g.153581381T>C , CM000685.1:g.153581381T>C	GRCh37
NC_000023.9:g.153234575T>C	NCBI36
NG_011506.1:g.26626A>G
NG_011506.2:g.26626A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6190A>G	ENSP00000353467.4:p.Thr2064Ala
ENST00000369850.10:c.6214A>G MANE Select	ENSP00000358866.3:p.Thr2072Ala
ENST00000369856.8:c.6133A>G	ENSP00000358872.4:p.Thr2045Ala
ENST00000422373.6:c.3161-338A>G	ENSP00000416926.2:n.3161-338A>G
ENST00000610817.5:c.6271A>G	ENSP00000480593.2:n.6271A>G
ENST00000673639.2:c.280-4323A>G
ENST00000676696.1:c.6493A>G	ENSP00000503392.1:n.6493A>G
ENST00000678304.1:n.1393A>G
ENST00000344736.8:c.6094A>G	ENSP00000358863.3:p.Thr2032Ala
ENST00000360319.8:c.6190A>G	ENSP00000353467.4:p.Thr2064Ala
ENST00000369850.7:c.6214A>G	ENSP00000358866.3:p.Thr2072Ala
ENST00000369856.7:c.6133A>G	ENSP00000358872.4:p.Thr2045Ala
ENST00000415241.1:c.416A>G
ENST00000420627.5:c.6170A>G	ENSP00000408921.1:n.6170A>G
ENST00000422373.5:c.6190A>G	ENSP00000416926.1:p.Thr2064Ala
ENST00000444578.1:c.157A>G	ENSP00000397824.1:p.Thr53Ala
ENST00000466325.1:n.353A>G
ENST00000490936.5:n.2203A>G
ENST00000610817.4:c.5844+380A>G	ENSP00000480593.1:n.5844+380A>G
NM_001110556.1:c.6214A>G	NP_001104026.1:p.Thr2072Ala
NM_001456.3:c.6190A>G	NP_001447.2:p.Thr2064Ala
XM_011531127.1:c.6118A>G	XP_011529429.1:p.Thr2040Ala
XM_011531128.1:c.6094A>G	XP_011529430.1:p.Thr2032Ala
XM_011531129.1:c.6040A>G	XP_011529431.1:p.Thr2014Ala
XM_011531130.1:c.6016A>G	XP_011529432.1:p.Thr2006Ala
XM_011531131.1:c.6013A>G	XP_011529433.1:p.Thr2005Ala
NM_001110556.2:c.6214A>G MANE Select	NP_001104026.1:p.Thr2072Ala
NM_001456.4:c.6190A>G	NP_001447.2:p.Thr2064Ala