Canonical Allele Identifier: CA2466653229

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353190G= , CM000685.2:g.154353190G=	GRCh38
NC_000023.10:g.153581558G= , CM000685.1:g.153581558G=	GRCh37
NC_000023.9:g.153234752G=	NCBI36
NG_011506.1:g.26449C=
NG_011506.2:g.26449C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6013C=	ENSP00000353467.4:p.Pro2005=
ENST00000369850.10:c.6037C= MANE Select	ENSP00000358866.3:p.Pro2013=
ENST00000369856.8:c.5956C=	ENSP00000358872.4:p.Pro1986=
ENST00000422373.6:c.3161-515C=	ENSP00000416926.2:n.3161-515C=
ENST00000610817.5:c.6094C=	ENSP00000480593.2:n.6094C=
ENST00000673639.2:c.280-4500C=
ENST00000676696.1:c.6316C=	ENSP00000503392.1:n.6316C=
ENST00000678304.1:n.1216C=
ENST00000344736.8:c.5917C=	ENSP00000358863.3:p.Pro1973=
ENST00000360319.8:c.6013C=	ENSP00000353467.4:p.Pro2005=
ENST00000369850.7:c.6037C=	ENSP00000358866.3:p.Pro2013=
ENST00000369856.7:c.5956C=	ENSP00000358872.4:p.Pro1986=
ENST00000415241.1:c.239C=
ENST00000420627.5:c.5993C=	ENSP00000408921.1:n.5993C=
ENST00000422373.5:c.6013C=	ENSP00000416926.1:p.Pro2005=
ENST00000466325.1:n.176C=
ENST00000490936.5:n.2026C=
ENST00000610817.4:c.5844+203C=	ENSP00000480593.1:n.5844+203C=
NM_001110556.1:c.6037C=	NP_001104026.1:p.Pro2013=
NM_001456.3:c.6013C=	NP_001447.2:p.Pro2005=
XM_011531127.1:c.5941C=	XP_011529429.1:p.Pro1981=
XM_011531128.1:c.5917C=	XP_011529430.1:p.Pro1973=
XM_011531129.1:c.5863C=	XP_011529431.1:p.Pro1955=
XM_011531130.1:c.5839C=	XP_011529432.1:p.Pro1947=
XM_011531131.1:c.5836C=	XP_011529433.1:p.Pro1946=
NM_001110556.2:c.6037C= MANE Select	NP_001104026.1:p.Pro2013=
NM_001456.4:c.6013C=	NP_001447.2:p.Pro2005=