Canonical Allele Identifier: CA415184314

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350175T>C , CM000685.2:g.154350175T>C	GRCh38
NC_000023.10:g.153578543T>C , CM000685.1:g.153578543T>C	GRCh37
NC_000023.9:g.153231737T>C	NCBI36
NG_011506.1:g.29464A>G
NG_011506.2:g.29464A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7165A>G	ENSP00000353467.4:p.Asn2389Asp
ENST00000369850.10:c.7189A>G MANE Select	ENSP00000358866.3:p.Asn2397Asp
ENST00000369856.8:c.7108A>G	ENSP00000358872.4:p.Asn2370Asp
ENST00000422373.6:c.3970A>G	ENSP00000416926.2:p.Asn1324Asp
ENST00000610817.5:c.7246A>G	ENSP00000480593.2:n.7246A>G
ENST00000673639.2:c.280-1485A>G
ENST00000676696.1:c.7468A>G	ENSP00000503392.1:n.7468A>G
ENST00000678304.1:n.2907A>G
ENST00000344736.8:c.7069A>G	ENSP00000358863.3:p.Asn2357Asp
ENST00000360319.8:c.7165A>G	ENSP00000353467.4:p.Asn2389Asp
ENST00000369850.7:c.7189A>G	ENSP00000358866.3:p.Asn2397Asp
ENST00000369856.7:c.7108A>G	ENSP00000358872.4:p.Asn2370Asp
ENST00000420627.5:c.7145A>G	ENSP00000408921.1:n.7145A>G
ENST00000422373.5:c.7165A>G	ENSP00000416926.1:p.Asn2389Asp
ENST00000462590.1:n.181A>G
ENST00000490936.5:n.4418A>G
ENST00000498411.1:n.68-1345A>G
ENST00000498491.5:n.230A>G
ENST00000610817.4:c.6193A>G	ENSP00000480593.1:p.Asn2065Asp
NM_001110556.1:c.7189A>G	NP_001104026.1:p.Asn2397Asp
NM_001456.3:c.7165A>G	NP_001447.2:p.Asn2389Asp
XM_011531127.1:c.7093A>G	XP_011529429.1:p.Asn2365Asp
XM_011531128.1:c.7069A>G	XP_011529430.1:p.Asn2357Asp
XM_011531129.1:c.7015A>G	XP_011529431.1:p.Asn2339Asp
XM_011531130.1:c.6991A>G	XP_011529432.1:p.Asn2331Asp
XM_011531131.1:c.6988A>G	XP_011529433.1:p.Asn2330Asp
NM_001110556.2:c.7189A>G MANE Select	NP_001104026.1:p.Asn2397Asp
NM_001456.4:c.7165A>G	NP_001447.2:p.Asn2389Asp