Canonical Allele Identifier: CA415193441

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581182T>A (hg19) ; chrX:g.154352814T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352814T>A , CM000685.2:g.154352814T>A	GRCh38
NC_000023.10:g.153581182T>A , CM000685.1:g.153581182T>A	GRCh37
NC_000023.9:g.153234376T>A	NCBI36
NG_011506.1:g.26825A>T
NG_011506.2:g.26825A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.6313A>T	ENSP00000353467.4:p.Asn2105Tyr
ENST00000369850.10:c.6337A>T MANE Select	ENSP00000358866.3:p.Asn2113Tyr
ENST00000369856.8:c.6256A>T	ENSP00000358872.4:p.Asn2086Tyr
ENST00000422373.6:c.3161-139A>T	ENSP00000416926.2:n.3161-139A>T
ENST00000610817.5:c.6394A>T	ENSP00000480593.2:n.6394A>T
ENST00000673639.2:c.280-4124A>T
ENST00000676696.1:c.6616A>T	ENSP00000503392.1:n.6616A>T
ENST00000678304.1:n.1516A>T
ENST00000344736.8:c.6217A>T	ENSP00000358863.3:p.Asn2073Tyr
ENST00000360319.8:c.6313A>T	ENSP00000353467.4:p.Asn2105Tyr
ENST00000369850.7:c.6337A>T	ENSP00000358866.3:p.Asn2113Tyr
ENST00000369856.7:c.6256A>T	ENSP00000358872.4:p.Asn2086Tyr
ENST00000415241.1:c.539A>T
ENST00000420627.5:c.6293A>T	ENSP00000408921.1:n.6293A>T
ENST00000422373.5:c.6313A>T	ENSP00000416926.1:p.Asn2105Tyr
ENST00000444578.1:c.280A>T	ENSP00000397824.1:p.Asn94Tyr
ENST00000466325.1:n.552A>T
ENST00000490936.5:n.2326A>T
ENST00000498411.1:n.67+3A>T
ENST00000610817.4:c.5844+579A>T	ENSP00000480593.1:n.5844+579A>T
NM_001110556.1:c.6337A>T	NP_001104026.1:p.Asn2113Tyr
NM_001456.3:c.6313A>T	NP_001447.2:p.Asn2105Tyr
XM_011531127.1:c.6241A>T	XP_011529429.1:p.Asn2081Tyr
XM_011531128.1:c.6217A>T	XP_011529430.1:p.Asn2073Tyr
XM_011531129.1:c.6163A>T	XP_011529431.1:p.Asn2055Tyr
XM_011531130.1:c.6139A>T	XP_011529432.1:p.Asn2047Tyr
XM_011531131.1:c.6136A>T	XP_011529433.1:p.Asn2046Tyr
NM_001110556.2:c.6337A>T MANE Select	NP_001104026.1:p.Asn2113Tyr
NM_001456.4:c.6313A>T	NP_001447.2:p.Asn2105Tyr