Canonical Allele Identifier: CA2466659021

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154367802T= , CM000685.2:g.154367802T=	GRCh38
NC_000023.10:g.153596170T= , CM000685.1:g.153596170T=	GRCh37
NC_000023.9:g.153249364T=	NCBI36
NG_011506.1:g.11837A=
NG_011506.2:g.11837A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.622+40A=	ENSP00000353467.4:n.622+40A=
ENST00000369850.10:c.622+40A= MANE Select	ENSP00000358866.3:n.622+40A=
ENST00000369856.8:c.541+40A=	ENSP00000358872.4:n.541+40A=
ENST00000422373.6:c.622+40A=	ENSP00000416926.2:n.622+40A=
ENST00000610817.5:c.622+40A=	ENSP00000480593.2:n.622+40A=
ENST00000676696.1:c.622+40A=	ENSP00000503392.1:n.622+40A=
ENST00000344736.8:c.622+40A=	ENSP00000358863.3:n.622+40A=
ENST00000360319.8:c.622+40A=	ENSP00000353467.4:n.622+40A=
ENST00000369850.7:c.622+40A=	ENSP00000358866.3:n.622+40A=
ENST00000369856.7:c.541+40A=	ENSP00000358872.4:n.541+40A=
ENST00000420627.5:c.580+40A=	ENSP00000408921.1:n.580+40A=
ENST00000422373.5:c.622+40A=	ENSP00000416926.1:n.622+40A=
ENST00000610817.4:c.541+40A=	ENSP00000480593.1:n.541+40A=
NM_001110556.1:c.622+40A=	NP_001104026.1:n.622+40A=
NM_001456.3:c.622+40A=	NP_001447.2:n.622+40A=
XM_011531127.1:c.622+40A=	XP_011529429.1:n.622+40A=
XM_011531128.1:c.622+40A=	XP_011529430.1:n.622+40A=
XM_011531129.1:c.622+40A=	XP_011529431.1:n.622+40A=
XM_011531130.1:c.622+40A=	XP_011529432.1:n.622+40A=
XM_011531131.1:c.622+40A=	XP_011529433.1:n.622+40A=
NM_001110556.2:c.622+40A= MANE Select	NP_001104026.1:n.622+40A=
NM_001456.4:c.622+40A=	NP_001447.2:n.622+40A=