Canonical Allele Identifier: CA10560350

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154354710G>A , CM000685.2:g.154354710G>A	GRCh38
NC_000023.10:g.153583078G>A , CM000685.1:g.153583078G>A	GRCh37
NC_000023.9:g.153236272G>A	NCBI36
NG_011506.1:g.24929C>T
NG_011506.2:g.24929C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5195C>T	ENSP00000353467.4:p.Ala1732Val
ENST00000369850.10:c.5219C>T MANE Select	ENSP00000358866.3:p.Ala1740Val
ENST00000369856.8:c.5138C>T	ENSP00000358872.4:p.Ala1713Val
ENST00000422373.6:c.3161-2035C>T	ENSP00000416926.2:n.3161-2035C>T
ENST00000610817.5:c.5276C>T	ENSP00000480593.2:n.5276C>T
ENST00000673639.2:c.280-6020C>T
ENST00000676696.1:c.5498C>T	ENSP00000503392.1:n.5498C>T
ENST00000678304.1:n.398C>T
ENST00000344736.8:c.5193+115C>T	ENSP00000358863.3:n.5193+115C>T
ENST00000360319.8:c.5195C>T	ENSP00000353467.4:p.Ala1732Val
ENST00000369850.7:c.5219C>T	ENSP00000358866.3:p.Ala1740Val
ENST00000369856.7:c.5138C>T	ENSP00000358872.4:p.Ala1713Val
ENST00000420627.5:c.5175C>T	ENSP00000408921.1:n.5175C>T
ENST00000422373.5:c.5195C>T	ENSP00000416926.1:p.Ala1732Val
ENST00000438732.2:c.67C>T
ENST00000490936.5:n.1208C>T
ENST00000610817.4:c.5138C>T	ENSP00000480593.1:p.Ala1713Val
NM_001110556.1:c.5219C>T	NP_001104026.1:p.Ala1740Val
NM_001456.3:c.5195C>T	NP_001447.2:p.Ala1732Val
XM_011531127.1:c.5217+115C>T	XP_011529429.1:n.5217+115C>T
XM_011531128.1:c.5193+115C>T	XP_011529430.1:n.5193+115C>T
XM_011531129.1:c.5219C>T	XP_011529431.1:p.Ala1740Val
XM_011531130.1:c.5195C>T	XP_011529432.1:p.Ala1732Val
XM_011531131.1:c.5018C>T	XP_011529433.1:p.Ala1673Val
NM_001110556.2:c.5219C>T MANE Select	NP_001104026.1:p.Ala1740Val
NM_001456.4:c.5195C>T	NP_001447.2:p.Ala1732Val