Canonical Allele Identifier: CA2466655180

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154358298G= , CM000685.2:g.154358298G=	GRCh38
NC_000023.10:g.153586666G= , CM000685.1:g.153586666G=	GRCh37
NC_000023.9:g.153239860G=	NCBI36
NG_011506.1:g.21341C=
NG_011506.2:g.21341C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.4656C=	ENSP00000353467.4:p.Gly1552=
ENST00000369850.10:c.4656C= MANE Select	ENSP00000358866.3:p.Gly1552=
ENST00000369856.8:c.4575C=	ENSP00000358872.4:p.Gly1525=
ENST00000422373.6:c.3160+3057C=	ENSP00000416926.2:n.3160+3057C=
ENST00000610817.5:c.4713C=	ENSP00000480593.2:n.4713C=
ENST00000673639.2:c.279+7138C=
ENST00000676696.1:c.4935C=	ENSP00000503392.1:n.4935C=
ENST00000678304.1:n.148+791C=
ENST00000344736.8:c.4656C=	ENSP00000358863.3:p.Gly1552=
ENST00000360319.8:c.4656C=	ENSP00000353467.4:p.Gly1552=
ENST00000369850.7:c.4656C=	ENSP00000358866.3:p.Gly1552=
ENST00000369856.7:c.4575C=	ENSP00000358872.4:p.Gly1525=
ENST00000420627.5:c.4612C=	ENSP00000408921.1:n.4612C=
ENST00000422373.5:c.4656C=	ENSP00000416926.1:p.Gly1552=
ENST00000466319.1:n.278C=
ENST00000490936.5:n.669C=
ENST00000610817.4:c.4575C=	ENSP00000480593.1:p.Gly1525=
NM_001110556.1:c.4656C=	NP_001104026.1:p.Gly1552=
NM_001456.3:c.4656C=	NP_001447.2:p.Gly1552=
XM_011531127.1:c.4656C=	XP_011529429.1:p.Gly1552=
XM_011531128.1:c.4656C=	XP_011529430.1:p.Gly1552=
XM_011531129.1:c.4656C=	XP_011529431.1:p.Gly1552=
XM_011531130.1:c.4656C=	XP_011529432.1:p.Gly1552=
XM_011531131.1:c.4455C=	XP_011529433.1:p.Gly1485=
NM_001110556.2:c.4656C= MANE Select	NP_001104026.1:p.Gly1552=
NM_001456.4:c.4656C=	NP_001447.2:p.Gly1552=