Canonical Allele Identifier: CA10560233

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353661C>T , CM000685.2:g.154353661C>T	GRCh38
NC_000023.10:g.153582029C>T , CM000685.1:g.153582029C>T	GRCh37
NC_000023.9:g.153235223C>T	NCBI36
NG_011506.1:g.25978G>A
NG_011506.2:g.25978G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001110556.2:c.5753G>A MANE Select	NP_001104026.1:p.Gly1918Glu
ENST00000369850.10:c.5753G>A MANE Select	ENSP00000358866.3:p.Gly1918Glu
NM_001110556.1:c.5753G>A	NP_001104026.1:p.Gly1918Glu
NM_001456.3:c.5729G>A	NP_001447.2:p.Gly1910Glu
NM_001456.4:c.5729G>A	NP_001447.2:p.Gly1910Glu
ENST00000344736.8:c.5633G>A	ENSP00000358863.3:p.Gly1878Glu
ENST00000360319.8:c.5729G>A	ENSP00000353467.4:p.Gly1910Glu
ENST00000360319.9:c.5729G>A	ENSP00000353467.4:p.Gly1910Glu
ENST00000369850.7:c.5753G>A	ENSP00000358866.3:p.Gly1918Glu
ENST00000369856.7:c.5672G>A	ENSP00000358872.4:p.Gly1891Glu
ENST00000369856.8:c.5672G>A	ENSP00000358872.4:p.Gly1891Glu
ENST00000420627.5:c.5709G>A	ENSP00000408921.1:n.5709G>A
ENST00000422373.5:c.5729G>A	ENSP00000416926.1:p.Gly1910Glu
ENST00000422373.6:c.3161-986G>A	ENSP00000416926.2:n.3161-986G>A
ENST00000438732.2:c.535-204G>A
ENST00000490936.5:n.1742G>A
ENST00000610817.4:c.5672G>A	ENSP00000480593.1:p.Gly1891Glu
ENST00000610817.5:c.5810G>A	ENSP00000480593.2:n.5810G>A
ENST00000673639.2:c.280-4971G>A
ENST00000676696.1:c.6032G>A	ENSP00000503392.1:n.6032G>A
ENST00000678304.1:n.932G>A
XM_011531127.1:c.5657G>A	XP_011529429.1:p.Gly1886Glu
XM_011531128.1:c.5633G>A	XP_011529430.1:p.Gly1878Glu
XM_011531129.1:c.5687-204G>A	XP_011529431.1:n.5687-204G>A
XM_011531130.1:c.5663-204G>A	XP_011529432.1:n.5663-204G>A
XM_011531131.1:c.5552G>A	XP_011529433.1:p.Gly1851Glu