Canonical Allele Identifier: CA10561121

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154365143C>T , CM000685.2:g.154365143C>T	GRCh38
NC_000023.10:g.153593511C>T , CM000685.1:g.153593511C>T	GRCh37
NC_000023.9:g.153246705C>T	NCBI36
NG_011506.1:g.14496G>A
NG_011506.2:g.14496G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001110556.2:c.1684G>A MANE Select	NP_001104026.1:p.Gly562Arg
ENST00000369850.10:c.1684G>A MANE Select	ENSP00000358866.3:p.Gly562Arg
NM_001110556.1:c.1684G>A	NP_001104026.1:p.Gly562Arg
NM_001456.3:c.1684G>A	NP_001447.2:p.Gly562Arg
NM_001456.4:c.1684G>A	NP_001447.2:p.Gly562Arg
ENST00000344736.8:c.1684G>A	ENSP00000358863.3:p.Gly562Arg
ENST00000360319.8:c.1684G>A	ENSP00000353467.4:p.Gly562Arg
ENST00000360319.9:c.1684G>A	ENSP00000353467.4:p.Gly562Arg
ENST00000369850.7:c.1684G>A	ENSP00000358866.3:p.Gly562Arg
ENST00000369856.7:c.1603G>A	ENSP00000358872.4:p.Gly535Arg
ENST00000369856.8:c.1603G>A	ENSP00000358872.4:p.Gly535Arg
ENST00000420627.5:c.1640G>A	ENSP00000408921.1:p.Arg547Gln
ENST00000422373.5:c.1684G>A	ENSP00000416926.1:p.Gly562Arg
ENST00000422373.6:c.1684G>A	ENSP00000416926.2:p.Gly562Arg
ENST00000465144.1:n.65G>A
ENST00000610817.4:c.1603G>A	ENSP00000480593.1:p.Gly535Arg
ENST00000610817.5:c.1741G>A	ENSP00000480593.2:n.1741G>A
ENST00000673639.2:c.279+293G>A
ENST00000676696.1:c.1963G>A	ENSP00000503392.1:n.1963G>A
XM_011531127.1:c.1684G>A	XP_011529429.1:p.Gly562Arg
XM_011531128.1:c.1684G>A	XP_011529430.1:p.Gly562Arg
XM_011531129.1:c.1684G>A	XP_011529431.1:p.Gly562Arg
XM_011531130.1:c.1684G>A	XP_011529432.1:p.Gly562Arg
XM_011531131.1:c.1483G>A	XP_011529433.1:p.Gly495Arg