Canonical Allele Identifier: CA415194033

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581232T>A (hg19) ; chrX:g.154352864T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352864T>A , CM000685.2:g.154352864T>A	GRCh38
NC_000023.10:g.153581232T>A , CM000685.1:g.153581232T>A	GRCh37
NC_000023.9:g.153234426T>A	NCBI36
NG_011506.1:g.26775A>T
NG_011506.2:g.26775A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6263A>T	ENSP00000353467.4:p.Asp2088Val
ENST00000369850.10:c.6287A>T MANE Select	ENSP00000358866.3:p.Asp2096Val
ENST00000369856.8:c.6206A>T	ENSP00000358872.4:p.Asp2069Val
ENST00000422373.6:c.3161-189A>T	ENSP00000416926.2:n.3161-189A>T
ENST00000610817.5:c.6344A>T	ENSP00000480593.2:n.6344A>T
ENST00000673639.2:c.280-4174A>T
ENST00000676696.1:c.6566A>T	ENSP00000503392.1:n.6566A>T
ENST00000678304.1:n.1466A>T
ENST00000344736.8:c.6167A>T	ENSP00000358863.3:p.Asp2056Val
ENST00000360319.8:c.6263A>T	ENSP00000353467.4:p.Asp2088Val
ENST00000369850.7:c.6287A>T	ENSP00000358866.3:p.Asp2096Val
ENST00000369856.7:c.6206A>T	ENSP00000358872.4:p.Asp2069Val
ENST00000415241.1:c.489A>T
ENST00000420627.5:c.6243A>T	ENSP00000408921.1:n.6243A>T
ENST00000422373.5:c.6263A>T	ENSP00000416926.1:p.Asp2088Val
ENST00000444578.1:c.230A>T	ENSP00000397824.1:p.Asp77Val
ENST00000466325.1:n.502A>T
ENST00000490936.5:n.2276A>T
ENST00000498411.1:n.20A>T
ENST00000610817.4:c.5844+529A>T	ENSP00000480593.1:n.5844+529A>T
NM_001110556.1:c.6287A>T	NP_001104026.1:p.Asp2096Val
NM_001456.3:c.6263A>T	NP_001447.2:p.Asp2088Val
XM_011531127.1:c.6191A>T	XP_011529429.1:p.Asp2064Val
XM_011531128.1:c.6167A>T	XP_011529430.1:p.Asp2056Val
XM_011531129.1:c.6113A>T	XP_011529431.1:p.Asp2038Val
XM_011531130.1:c.6089A>T	XP_011529432.1:p.Asp2030Val
XM_011531131.1:c.6086A>T	XP_011529433.1:p.Asp2029Val
NM_001110556.2:c.6287A>T MANE Select	NP_001104026.1:p.Asp2096Val
NM_001456.4:c.6263A>T	NP_001447.2:p.Asp2088Val