Canonical Allele Identifier: CA10560082

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352574C>T , CM000685.2:g.154352574C>T	GRCh38
NC_000023.10:g.153580942C>T , CM000685.1:g.153580942C>T	GRCh37
NC_000023.9:g.153234136C>T	NCBI36
NG_011506.1:g.27065G>A
NG_011506.2:g.27065G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6457G>A	ENSP00000353467.4:p.Asp2153Asn
ENST00000369850.10:c.6481G>A MANE Select	ENSP00000358866.3:p.Asp2161Asn
ENST00000369856.8:c.6400G>A	ENSP00000358872.4:p.Asp2134Asn
ENST00000422373.6:c.3262G>A	ENSP00000416926.2:p.Asp1088Asn
ENST00000610817.5:c.6538G>A	ENSP00000480593.2:n.6538G>A
ENST00000673639.2:c.280-3884G>A
ENST00000676696.1:c.6760G>A	ENSP00000503392.1:n.6760G>A
ENST00000678304.1:n.1660G>A
ENST00000344736.8:c.6361G>A	ENSP00000358863.3:p.Asp2121Asn
ENST00000360319.8:c.6457G>A	ENSP00000353467.4:p.Asp2153Asn
ENST00000369850.7:c.6481G>A	ENSP00000358866.3:p.Asp2161Asn
ENST00000369856.7:c.6400G>A	ENSP00000358872.4:p.Asp2134Asn
ENST00000415241.1:c.683G>A
ENST00000420627.5:c.6437G>A	ENSP00000408921.1:n.6437G>A
ENST00000422373.5:c.6457G>A	ENSP00000416926.1:p.Asp2153Asn
ENST00000444578.1:c.323-127G>A	ENSP00000397824.1:n.323-127G>A
ENST00000466325.1:n.792G>A
ENST00000474358.5:n.114G>A
ENST00000490936.5:n.2470G>A
ENST00000498411.1:n.67+243G>A
ENST00000610817.4:c.5845-624G>A	ENSP00000480593.1:n.5845-624G>A
NM_001110556.1:c.6481G>A	NP_001104026.1:p.Asp2161Asn
NM_001456.3:c.6457G>A	NP_001447.2:p.Asp2153Asn
XM_011531127.1:c.6385G>A	XP_011529429.1:p.Asp2129Asn
XM_011531128.1:c.6361G>A	XP_011529430.1:p.Asp2121Asn
XM_011531129.1:c.6307G>A	XP_011529431.1:p.Asp2103Asn
XM_011531130.1:c.6283G>A	XP_011529432.1:p.Asp2095Asn
XM_011531131.1:c.6280G>A	XP_011529433.1:p.Asp2094Asn
NM_001110556.2:c.6481G>A MANE Select	NP_001104026.1:p.Asp2161Asn
NM_001456.4:c.6457G>A	NP_001447.2:p.Asp2153Asn