Canonical Allele Identifier: CA519276197

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154348924C>T , CM000685.2:g.154348924C>T	GRCh38
NC_000023.10:g.153577292C>T , CM000685.1:g.153577292C>T	GRCh37
NC_000023.9:g.153230486C>T	NCBI36
NG_011506.1:g.30715G>A
NG_011506.2:g.30715G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7845G>A	ENSP00000353467.4:p.Lys2615=
ENST00000369850.10:c.7869G>A MANE Select	ENSP00000358866.3:p.Lys2623=
ENST00000369856.8:c.7788G>A	ENSP00000358872.4:p.Lys2596=
ENST00000422373.6:c.4650G>A	ENSP00000416926.2:p.Lys1550=
ENST00000610817.5:c.7926G>A	ENSP00000480593.2:n.7926G>A
ENST00000673639.2:c.280-234G>A
ENST00000676696.1:c.8148G>A	ENSP00000503392.1:n.8148G>A
ENST00000678304.1:n.3587G>A
ENST00000344736.8:c.7749G>A	ENSP00000358863.3:p.Lys2583=
ENST00000360319.8:c.7845G>A	ENSP00000353467.4:p.Lys2615=
ENST00000369850.7:c.7869G>A	ENSP00000358866.3:p.Lys2623=
ENST00000369856.7:c.7788G>A	ENSP00000358872.4:p.Lys2596=
ENST00000420627.5:c.7825G>A	ENSP00000408921.1:n.7825G>A
ENST00000422373.5:c.7845G>A	ENSP00000416926.1:p.Lys2615=
ENST00000462590.1:n.1024G>A
ENST00000490936.5:n.5098G>A
ENST00000498411.1:n.68-94G>A
ENST00000498491.5:n.910G>A
ENST00000610817.4:c.6873G>A	ENSP00000480593.1:p.Lys2291=
NM_001110556.1:c.7869G>A	NP_001104026.1:p.Lys2623=
NM_001456.3:c.7845G>A	NP_001447.2:p.Lys2615=
XM_011531127.1:c.7773G>A	XP_011529429.1:p.Lys2591=
XM_011531128.1:c.7749G>A	XP_011529430.1:p.Lys2583=
XM_011531129.1:c.7695G>A	XP_011529431.1:p.Lys2565=
XM_011531130.1:c.7671G>A	XP_011529432.1:p.Lys2557=
XM_011531131.1:c.7668G>A	XP_011529433.1:p.Lys2556=
NM_001110556.2:c.7869G>A MANE Select	NP_001104026.1:p.Lys2623=
NM_001456.4:c.7845G>A	NP_001447.2:p.Lys2615=