Canonical Allele Identifier: CA415184413

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350186A>T , CM000685.2:g.154350186A>T	GRCh38
NC_000023.10:g.153578554A>T , CM000685.1:g.153578554A>T	GRCh37
NC_000023.9:g.153231748A>T	NCBI36
NG_011506.1:g.29453T>A
NG_011506.2:g.29453T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7154T>A	ENSP00000353467.4:p.Ile2385Asn
ENST00000369850.10:c.7178T>A MANE Select	ENSP00000358866.3:p.Ile2393Asn
ENST00000369856.8:c.7097T>A	ENSP00000358872.4:p.Ile2366Asn
ENST00000422373.6:c.3959T>A	ENSP00000416926.2:p.Ile1320Asn
ENST00000610817.5:c.7235T>A	ENSP00000480593.2:n.7235T>A
ENST00000673639.2:c.280-1496T>A
ENST00000676696.1:c.7457T>A	ENSP00000503392.1:n.7457T>A
ENST00000678304.1:n.2896T>A
ENST00000344736.8:c.7058T>A	ENSP00000358863.3:p.Ile2353Asn
ENST00000360319.8:c.7154T>A	ENSP00000353467.4:p.Ile2385Asn
ENST00000369850.7:c.7178T>A	ENSP00000358866.3:p.Ile2393Asn
ENST00000369856.7:c.7097T>A	ENSP00000358872.4:p.Ile2366Asn
ENST00000420627.5:c.7134T>A	ENSP00000408921.1:n.7134T>A
ENST00000422373.5:c.7154T>A	ENSP00000416926.1:p.Ile2385Asn
ENST00000462590.1:n.170T>A
ENST00000490936.5:n.4407T>A
ENST00000498411.1:n.68-1356T>A
ENST00000498491.5:n.219T>A
ENST00000610817.4:c.6182T>A	ENSP00000480593.1:p.Ile2061Asn
NM_001110556.1:c.7178T>A	NP_001104026.1:p.Ile2393Asn
NM_001456.3:c.7154T>A	NP_001447.2:p.Ile2385Asn
XM_011531127.1:c.7082T>A	XP_011529429.1:p.Ile2361Asn
XM_011531128.1:c.7058T>A	XP_011529430.1:p.Ile2353Asn
XM_011531129.1:c.7004T>A	XP_011529431.1:p.Ile2335Asn
XM_011531130.1:c.6980T>A	XP_011529432.1:p.Ile2327Asn
XM_011531131.1:c.6977T>A	XP_011529433.1:p.Ile2326Asn
NM_001110556.2:c.7178T>A MANE Select	NP_001104026.1:p.Ile2393Asn
NM_001456.4:c.7154T>A	NP_001447.2:p.Ile2385Asn