Canonical Allele Identifier: CA2466653162

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353011G= , CM000685.2:g.154353011G=	GRCh38
NC_000023.10:g.153581379G= , CM000685.1:g.153581379G=	GRCh37
NC_000023.9:g.153234573G=	NCBI36
NG_011506.1:g.26628C=
NG_011506.2:g.26628C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6192C=	ENSP00000353467.4:p.Thr2064=
ENST00000369850.10:c.6216C= MANE Select	ENSP00000358866.3:p.Thr2072=
ENST00000369856.8:c.6135C=	ENSP00000358872.4:p.Thr2045=
ENST00000422373.6:c.3161-336C=	ENSP00000416926.2:n.3161-336C=
ENST00000610817.5:c.6273C=	ENSP00000480593.2:n.6273C=
ENST00000673639.2:c.280-4321C=
ENST00000676696.1:c.6495C=	ENSP00000503392.1:n.6495C=
ENST00000678304.1:n.1395C=
ENST00000344736.8:c.6096C=	ENSP00000358863.3:p.Thr2032=
ENST00000360319.8:c.6192C=	ENSP00000353467.4:p.Thr2064=
ENST00000369850.7:c.6216C=	ENSP00000358866.3:p.Thr2072=
ENST00000369856.7:c.6135C=	ENSP00000358872.4:p.Thr2045=
ENST00000415241.1:c.418C=
ENST00000420627.5:c.6172C=	ENSP00000408921.1:n.6172C=
ENST00000422373.5:c.6192C=	ENSP00000416926.1:p.Thr2064=
ENST00000444578.1:c.159C=	ENSP00000397824.1:p.Thr53=
ENST00000466325.1:n.355C=
ENST00000490936.5:n.2205C=
ENST00000610817.4:c.5844+382C=	ENSP00000480593.1:n.5844+382C=
NM_001110556.1:c.6216C=	NP_001104026.1:p.Thr2072=
NM_001456.3:c.6192C=	NP_001447.2:p.Thr2064=
XM_011531127.1:c.6120C=	XP_011529429.1:p.Thr2040=
XM_011531128.1:c.6096C=	XP_011529430.1:p.Thr2032=
XM_011531129.1:c.6042C=	XP_011529431.1:p.Thr2014=
XM_011531130.1:c.6018C=	XP_011529432.1:p.Thr2006=
XM_011531131.1:c.6015C=	XP_011529433.1:p.Thr2005=
NM_001110556.2:c.6216C= MANE Select	NP_001104026.1:p.Thr2072=
NM_001456.4:c.6192C=	NP_001447.2:p.Thr2064=