Canonical Allele Identifier: CA2466653033

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352695C= , CM000685.2:g.154352695C=	GRCh38
NC_000023.10:g.153581063C= , CM000685.1:g.153581063C=	GRCh37
NC_000023.9:g.153234257C=	NCBI36
NG_011506.1:g.26944G=
NG_011506.2:g.26944G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6356-20G=	ENSP00000353467.4:n.6356-20G=
ENST00000369850.10:c.6380-20G= MANE Select	ENSP00000358866.3:n.6380-20G=
ENST00000369856.8:c.6299-20G=	ENSP00000358872.4:n.6299-20G=
ENST00000422373.6:c.3161-20G=	ENSP00000416926.2:n.3161-20G=
ENST00000610817.5:c.6437-20G=	ENSP00000480593.2:n.6437-20G=
ENST00000673639.2:c.280-4005G=
ENST00000676696.1:c.6659-20G=	ENSP00000503392.1:n.6659-20G=
ENST00000678304.1:n.1559-20G=
ENST00000344736.8:c.6260-20G=	ENSP00000358863.3:n.6260-20G=
ENST00000360319.8:c.6356-20G=	ENSP00000353467.4:n.6356-20G=
ENST00000369850.7:c.6380-20G=	ENSP00000358866.3:n.6380-20G=
ENST00000369856.7:c.6299-20G=	ENSP00000358872.4:n.6299-20G=
ENST00000415241.1:c.582-20G=
ENST00000420627.5:c.6336-20G=	ENSP00000408921.1:n.6336-20G=
ENST00000422373.5:c.6356-20G=	ENSP00000416926.1:n.6356-20G=
ENST00000444578.1:c.322+77G=	ENSP00000397824.1:n.322+77G=
ENST00000466325.1:n.671G=
ENST00000474358.5:n.13-20G=
ENST00000490936.5:n.2369-20G=
ENST00000498411.1:n.67+122G=
ENST00000610817.4:c.5844+698G=	ENSP00000480593.1:n.5844+698G=
NM_001110556.1:c.6380-20G=	NP_001104026.1:n.6380-20G=
NM_001456.3:c.6356-20G=	NP_001447.2:n.6356-20G=
XM_011531127.1:c.6284-20G=	XP_011529429.1:n.6284-20G=
XM_011531128.1:c.6260-20G=	XP_011529430.1:n.6260-20G=
XM_011531129.1:c.6206-20G=	XP_011529431.1:n.6206-20G=
XM_011531130.1:c.6182-20G=	XP_011529432.1:n.6182-20G=
XM_011531131.1:c.6179-20G=	XP_011529433.1:n.6179-20G=
NM_001110556.2:c.6380-20G= MANE Select	NP_001104026.1:n.6380-20G=
NM_001456.4:c.6356-20G=	NP_001447.2:n.6356-20G=