Canonical Allele Identifier: CA415193266

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581170T>C (hg19) ; chrX:g.154352802T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352802T>C , CM000685.2:g.154352802T>C	GRCh38
NC_000023.10:g.153581170T>C , CM000685.1:g.153581170T>C	GRCh37
NC_000023.9:g.153234364T>C	NCBI36
NG_011506.1:g.26837A>G
NG_011506.2:g.26837A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6325A>G	ENSP00000353467.4:p.Asn2109Asp
ENST00000369850.10:c.6349A>G MANE Select	ENSP00000358866.3:p.Asn2117Asp
ENST00000369856.8:c.6268A>G	ENSP00000358872.4:p.Asn2090Asp
ENST00000422373.6:c.3161-127A>G	ENSP00000416926.2:n.3161-127A>G
ENST00000610817.5:c.6406A>G	ENSP00000480593.2:n.6406A>G
ENST00000673639.2:c.280-4112A>G
ENST00000676696.1:c.6628A>G	ENSP00000503392.1:n.6628A>G
ENST00000678304.1:n.1528A>G
ENST00000344736.8:c.6229A>G	ENSP00000358863.3:p.Asn2077Asp
ENST00000360319.8:c.6325A>G	ENSP00000353467.4:p.Asn2109Asp
ENST00000369850.7:c.6349A>G	ENSP00000358866.3:p.Asn2117Asp
ENST00000369856.7:c.6268A>G	ENSP00000358872.4:p.Asn2090Asp
ENST00000415241.1:c.551A>G
ENST00000420627.5:c.6305A>G	ENSP00000408921.1:n.6305A>G
ENST00000422373.5:c.6325A>G	ENSP00000416926.1:p.Asn2109Asp
ENST00000444578.1:c.292A>G	ENSP00000397824.1:p.Asn98Asp
ENST00000466325.1:n.564A>G
ENST00000490936.5:n.2338A>G
ENST00000498411.1:n.67+15A>G
ENST00000610817.4:c.5844+591A>G	ENSP00000480593.1:n.5844+591A>G
NM_001110556.1:c.6349A>G	NP_001104026.1:p.Asn2117Asp
NM_001456.3:c.6325A>G	NP_001447.2:p.Asn2109Asp
XM_011531127.1:c.6253A>G	XP_011529429.1:p.Asn2085Asp
XM_011531128.1:c.6229A>G	XP_011529430.1:p.Asn2077Asp
XM_011531129.1:c.6175A>G	XP_011529431.1:p.Asn2059Asp
XM_011531130.1:c.6151A>G	XP_011529432.1:p.Asn2051Asp
XM_011531131.1:c.6148A>G	XP_011529433.1:p.Asn2050Asp
NM_001110556.2:c.6349A>G MANE Select	NP_001104026.1:p.Asn2117Asp
NM_001456.4:c.6325A>G	NP_001447.2:p.Asn2109Asp