Canonical Allele Identifier: CA2466653274

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353300G= , CM000685.2:g.154353300G=	GRCh38
NC_000023.10:g.153581668G= , CM000685.1:g.153581668G=	GRCh37
NC_000023.9:g.153234862G=	NCBI36
NG_011506.1:g.26339C=
NG_011506.2:g.26339C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5994C=	ENSP00000353467.4:p.His1998=
ENST00000369850.10:c.6018C= MANE Select	ENSP00000358866.3:p.His2006=
ENST00000369856.8:c.5937C=	ENSP00000358872.4:p.His1979=
ENST00000422373.6:c.3161-625C=	ENSP00000416926.2:n.3161-625C=
ENST00000610817.5:c.6075C=	ENSP00000480593.2:n.6075C=
ENST00000673639.2:c.280-4610C=
ENST00000676696.1:c.6297C=	ENSP00000503392.1:n.6297C=
ENST00000678304.1:n.1197C=
ENST00000344736.8:c.5898C=	ENSP00000358863.3:p.His1966=
ENST00000360319.8:c.5994C=	ENSP00000353467.4:p.His1998=
ENST00000369850.7:c.6018C=	ENSP00000358866.3:p.His2006=
ENST00000369856.7:c.5937C=	ENSP00000358872.4:p.His1979=
ENST00000415241.1:c.203C=
ENST00000420627.5:c.5974C=	ENSP00000408921.1:n.5974C=
ENST00000422373.5:c.5994C=	ENSP00000416926.1:p.His1998=
ENST00000438732.2:c.692C=
ENST00000466325.1:n.157C=
ENST00000490936.5:n.2007C=
ENST00000610817.4:c.5844+93C=	ENSP00000480593.1:n.5844+93C=
NM_001110556.1:c.6018C=	NP_001104026.1:p.His2006=
NM_001456.3:c.5994C=	NP_001447.2:p.His1998=
XM_011531127.1:c.5922C=	XP_011529429.1:p.His1974=
XM_011531128.1:c.5898C=	XP_011529430.1:p.His1966=
XM_011531129.1:c.5844C=	XP_011529431.1:p.His1948=
XM_011531130.1:c.5820C=	XP_011529432.1:p.His1940=
XM_011531131.1:c.5817C=	XP_011529433.1:p.His1939=
NM_001110556.2:c.6018C= MANE Select	NP_001104026.1:p.His2006=
NM_001456.4:c.5994C=	NP_001447.2:p.His1998=