Canonical Allele Identifier: CA2466653204

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353119C= , CM000685.2:g.154353119C=	GRCh38
NC_000023.10:g.153581487C= , CM000685.1:g.153581487C=	GRCh37
NC_000023.9:g.153234681C=	NCBI36
NG_011506.1:g.26520G=
NG_011506.2:g.26520G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6084G=	ENSP00000353467.4:p.Pro2028=
ENST00000369850.10:c.6108G= MANE Select	ENSP00000358866.3:p.Pro2036=
ENST00000369856.8:c.6027G=	ENSP00000358872.4:p.Pro2009=
ENST00000422373.6:c.3161-444G=	ENSP00000416926.2:n.3161-444G=
ENST00000610817.5:c.6165G=	ENSP00000480593.2:n.6165G=
ENST00000673639.2:c.280-4429G=
ENST00000676696.1:c.6387G=	ENSP00000503392.1:n.6387G=
ENST00000678304.1:n.1287G=
ENST00000344736.8:c.5988G=	ENSP00000358863.3:p.Pro1996=
ENST00000360319.8:c.6084G=	ENSP00000353467.4:p.Pro2028=
ENST00000369850.7:c.6108G=	ENSP00000358866.3:p.Pro2036=
ENST00000369856.7:c.6027G=	ENSP00000358872.4:p.Pro2009=
ENST00000415241.1:c.310G=
ENST00000420627.5:c.6064G=	ENSP00000408921.1:n.6064G=
ENST00000422373.5:c.6084G=	ENSP00000416926.1:p.Pro2028=
ENST00000444578.1:c.51G=	ENSP00000397824.1:p.Pro17=
ENST00000466325.1:n.247G=
ENST00000490936.5:n.2097G=
ENST00000610817.4:c.5844+274G=	ENSP00000480593.1:n.5844+274G=
NM_001110556.1:c.6108G=	NP_001104026.1:p.Pro2036=
NM_001456.3:c.6084G=	NP_001447.2:p.Pro2028=
XM_011531127.1:c.6012G=	XP_011529429.1:p.Pro2004=
XM_011531128.1:c.5988G=	XP_011529430.1:p.Pro1996=
XM_011531129.1:c.5934G=	XP_011529431.1:p.Pro1978=
XM_011531130.1:c.5910G=	XP_011529432.1:p.Pro1970=
XM_011531131.1:c.5907G=	XP_011529433.1:p.Pro1969=
NM_001110556.2:c.6108G= MANE Select	NP_001104026.1:p.Pro2036=
NM_001456.4:c.6084G=	NP_001447.2:p.Pro2028=