Canonical Allele Identifier: CA10560232

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353650C>T , CM000685.2:g.154353650C>T	GRCh38
NC_000023.10:g.153582018C>T , CM000685.1:g.153582018C>T	GRCh37
NC_000023.9:g.153235212C>T	NCBI36
NG_011506.1:g.25989G>A
NG_011506.2:g.25989G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001110556.2:c.5764G>A MANE Select	NP_001104026.1:p.Val1922Met
ENST00000369850.10:c.5764G>A MANE Select	ENSP00000358866.3:p.Val1922Met
NM_001110556.1:c.5764G>A	NP_001104026.1:p.Val1922Met
NM_001456.3:c.5740G>A	NP_001447.2:p.Val1914Met
NM_001456.4:c.5740G>A	NP_001447.2:p.Val1914Met
ENST00000344736.8:c.5644G>A	ENSP00000358863.3:p.Val1882Met
ENST00000360319.8:c.5740G>A	ENSP00000353467.4:p.Val1914Met
ENST00000360319.9:c.5740G>A	ENSP00000353467.4:p.Val1914Met
ENST00000369850.7:c.5764G>A	ENSP00000358866.3:p.Val1922Met
ENST00000369856.7:c.5683G>A	ENSP00000358872.4:p.Val1895Met
ENST00000369856.8:c.5683G>A	ENSP00000358872.4:p.Val1895Met
ENST00000420627.5:c.5720G>A	ENSP00000408921.1:n.5720G>A
ENST00000422373.5:c.5740G>A	ENSP00000416926.1:p.Val1914Met
ENST00000422373.6:c.3161-975G>A	ENSP00000416926.2:n.3161-975G>A
ENST00000438732.2:c.535-193G>A
ENST00000490936.5:n.1753G>A
ENST00000610817.4:c.5683G>A	ENSP00000480593.1:p.Val1895Met
ENST00000610817.5:c.5821G>A	ENSP00000480593.2:n.5821G>A
ENST00000673639.2:c.280-4960G>A
ENST00000676696.1:c.6043G>A	ENSP00000503392.1:n.6043G>A
ENST00000678304.1:n.943G>A
XM_011531127.1:c.5668G>A	XP_011529429.1:p.Val1890Met
XM_011531128.1:c.5644G>A	XP_011529430.1:p.Val1882Met
XM_011531129.1:c.5687-193G>A	XP_011529431.1:n.5687-193G>A
XM_011531130.1:c.5663-193G>A	XP_011529432.1:n.5663-193G>A
XM_011531131.1:c.5563G>A	XP_011529433.1:p.Val1855Met