Canonical Allele Identifier: CA2466653082

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352827G= , CM000685.2:g.154352827G=	GRCh38
NC_000023.10:g.153581195G= , CM000685.1:g.153581195G=	GRCh37
NC_000023.9:g.153234389G=	NCBI36
NG_011506.1:g.26812C=
NG_011506.2:g.26812C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6300C=	ENSP00000353467.4:p.Pro2100=
ENST00000369850.10:c.6324C= MANE Select	ENSP00000358866.3:p.Pro2108=
ENST00000369856.8:c.6243C=	ENSP00000358872.4:p.Pro2081=
ENST00000422373.6:c.3161-152C=	ENSP00000416926.2:n.3161-152C=
ENST00000610817.5:c.6381C=	ENSP00000480593.2:n.6381C=
ENST00000673639.2:c.280-4137C=
ENST00000676696.1:c.6603C=	ENSP00000503392.1:n.6603C=
ENST00000678304.1:n.1503C=
ENST00000344736.8:c.6204C=	ENSP00000358863.3:p.Pro2068=
ENST00000360319.8:c.6300C=	ENSP00000353467.4:p.Pro2100=
ENST00000369850.7:c.6324C=	ENSP00000358866.3:p.Pro2108=
ENST00000369856.7:c.6243C=	ENSP00000358872.4:p.Pro2081=
ENST00000415241.1:c.526C=
ENST00000420627.5:c.6280C=	ENSP00000408921.1:n.6280C=
ENST00000422373.5:c.6300C=	ENSP00000416926.1:p.Pro2100=
ENST00000444578.1:c.267C=	ENSP00000397824.1:p.Pro89=
ENST00000466325.1:n.539C=
ENST00000490936.5:n.2313C=
ENST00000498411.1:n.57C=
ENST00000610817.4:c.5844+566C=	ENSP00000480593.1:n.5844+566C=
NM_001110556.1:c.6324C=	NP_001104026.1:p.Pro2108=
NM_001456.3:c.6300C=	NP_001447.2:p.Pro2100=
XM_011531127.1:c.6228C=	XP_011529429.1:p.Pro2076=
XM_011531128.1:c.6204C=	XP_011529430.1:p.Pro2068=
XM_011531129.1:c.6150C=	XP_011529431.1:p.Pro2050=
XM_011531130.1:c.6126C=	XP_011529432.1:p.Pro2042=
XM_011531131.1:c.6123C=	XP_011529433.1:p.Pro2041=
NM_001110556.2:c.6324C= MANE Select	NP_001104026.1:p.Pro2108=
NM_001456.4:c.6300C=	NP_001447.2:p.Pro2100=