Canonical Allele Identifier: CA415192563

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581022A>G (hg19) ; chrX:g.154352654A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352654A>G , CM000685.2:g.154352654A>G	GRCh38
NC_000023.10:g.153581022A>G , CM000685.1:g.153581022A>G	GRCh37
NC_000023.9:g.153234216A>G	NCBI36
NG_011506.1:g.26985T>C
NG_011506.2:g.26985T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6377T>C	ENSP00000353467.4:p.Val2126Ala
ENST00000369850.10:c.6401T>C MANE Select	ENSP00000358866.3:p.Val2134Ala
ENST00000369856.8:c.6320T>C	ENSP00000358872.4:p.Val2107Ala
ENST00000422373.6:c.3182T>C	ENSP00000416926.2:p.Val1061Ala
ENST00000610817.5:c.6458T>C	ENSP00000480593.2:n.6458T>C
ENST00000673639.2:c.280-3964T>C
ENST00000676696.1:c.6680T>C	ENSP00000503392.1:n.6680T>C
ENST00000678304.1:n.1580T>C
ENST00000344736.8:c.6281T>C	ENSP00000358863.3:p.Val2094Ala
ENST00000360319.8:c.6377T>C	ENSP00000353467.4:p.Val2126Ala
ENST00000369850.7:c.6401T>C	ENSP00000358866.3:p.Val2134Ala
ENST00000369856.7:c.6320T>C	ENSP00000358872.4:p.Val2107Ala
ENST00000415241.1:c.603T>C
ENST00000420627.5:c.6357T>C	ENSP00000408921.1:n.6357T>C
ENST00000422373.5:c.6377T>C	ENSP00000416926.1:p.Val2126Ala
ENST00000444578.1:c.322+118T>C	ENSP00000397824.1:n.322+118T>C
ENST00000466325.1:n.712T>C
ENST00000474358.5:n.34T>C
ENST00000490936.5:n.2390T>C
ENST00000498411.1:n.67+163T>C
ENST00000610817.4:c.5845-704T>C	ENSP00000480593.1:n.5845-704T>C
NM_001110556.1:c.6401T>C	NP_001104026.1:p.Val2134Ala
NM_001456.3:c.6377T>C	NP_001447.2:p.Val2126Ala
XM_011531127.1:c.6305T>C	XP_011529429.1:p.Val2102Ala
XM_011531128.1:c.6281T>C	XP_011529430.1:p.Val2094Ala
XM_011531129.1:c.6227T>C	XP_011529431.1:p.Val2076Ala
XM_011531130.1:c.6203T>C	XP_011529432.1:p.Val2068Ala
XM_011531131.1:c.6200T>C	XP_011529433.1:p.Val2067Ala
NM_001110556.2:c.6401T>C MANE Select	NP_001104026.1:p.Val2134Ala
NM_001456.4:c.6377T>C	NP_001447.2:p.Val2126Ala