Canonical Allele Identifier: CA2466653123

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352930G= , CM000685.2:g.154352930G=	GRCh38
NC_000023.10:g.153581298G= , CM000685.1:g.153581298G=	GRCh37
NC_000023.9:g.153234492G=	NCBI36
NG_011506.1:g.26709C=
NG_011506.2:g.26709C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6203-6C=	ENSP00000353467.4:n.6203-6C=
ENST00000369850.10:c.6227-6C= MANE Select	ENSP00000358866.3:n.6227-6C=
ENST00000369856.8:c.6146-6C=	ENSP00000358872.4:n.6146-6C=
ENST00000422373.6:c.3161-255C=	ENSP00000416926.2:n.3161-255C=
ENST00000610817.5:c.6284-6C=	ENSP00000480593.2:n.6284-6C=
ENST00000673639.2:c.280-4240C=
ENST00000676696.1:c.6506-6C=	ENSP00000503392.1:n.6506-6C=
ENST00000678304.1:n.1406-6C=
ENST00000344736.8:c.6107-6C=	ENSP00000358863.3:n.6107-6C=
ENST00000360319.8:c.6203-6C=	ENSP00000353467.4:n.6203-6C=
ENST00000369850.7:c.6227-6C=	ENSP00000358866.3:n.6227-6C=
ENST00000369856.7:c.6146-6C=	ENSP00000358872.4:n.6146-6C=
ENST00000415241.1:c.429-6C=
ENST00000420627.5:c.6183-6C=	ENSP00000408921.1:n.6183-6C=
ENST00000422373.5:c.6203-6C=	ENSP00000416926.1:n.6203-6C=
ENST00000444578.1:c.170-6C=	ENSP00000397824.1:n.170-6C=
ENST00000466325.1:n.436C=
ENST00000490936.5:n.2216-6C=
ENST00000610817.4:c.5844+463C=	ENSP00000480593.1:n.5844+463C=
NM_001110556.1:c.6227-6C=	NP_001104026.1:n.6227-6C=
NM_001456.3:c.6203-6C=	NP_001447.2:n.6203-6C=
XM_011531127.1:c.6131-6C=	XP_011529429.1:n.6131-6C=
XM_011531128.1:c.6107-6C=	XP_011529430.1:n.6107-6C=
XM_011531129.1:c.6053-6C=	XP_011529431.1:n.6053-6C=
XM_011531130.1:c.6029-6C=	XP_011529432.1:n.6029-6C=
XM_011531131.1:c.6026-6C=	XP_011529433.1:n.6026-6C=
NM_001110556.2:c.6227-6C= MANE Select	NP_001104026.1:n.6227-6C=
NM_001456.4:c.6203-6C=	NP_001447.2:n.6203-6C=