Canonical Allele Identifier: CA10559952

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350915C>T , CM000685.2:g.154350915C>T	GRCh38
NC_000023.10:g.153579283C>T , CM000685.1:g.153579283C>T	GRCh37
NC_000023.9:g.153232477C>T	NCBI36
NG_011506.1:g.28724G>A
NG_011506.2:g.28724G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001110556.2:c.7150G>A MANE Select	NP_001104026.1:p.Asp2384Asn
ENST00000369850.10:c.7150G>A MANE Select	ENSP00000358866.3:p.Asp2384Asn
NM_001110556.1:c.7150G>A	NP_001104026.1:p.Asp2384Asn
NM_001456.3:c.7126G>A	NP_001447.2:p.Asp2376Asn
NM_001456.4:c.7126G>A	NP_001447.2:p.Asp2376Asn
ENST00000344736.8:c.7030G>A	ENSP00000358863.3:p.Asp2344Asn
ENST00000360319.8:c.7126G>A	ENSP00000353467.4:p.Asp2376Asn
ENST00000360319.9:c.7126G>A	ENSP00000353467.4:p.Asp2376Asn
ENST00000369850.7:c.7150G>A	ENSP00000358866.3:p.Asp2384Asn
ENST00000369856.7:c.7069G>A	ENSP00000358872.4:p.Asp2357Asn
ENST00000369856.8:c.7069G>A	ENSP00000358872.4:p.Asp2357Asn
ENST00000420627.5:c.7106G>A	ENSP00000408921.1:n.7106G>A
ENST00000422373.5:c.7126G>A	ENSP00000416926.1:p.Asp2376Asn
ENST00000422373.6:c.3931G>A	ENSP00000416926.2:p.Asp1311Asn
ENST00000490936.5:n.3678G>A
ENST00000498411.1:n.67+1902G>A
ENST00000498491.5:n.191G>A
ENST00000610817.4:c.6154G>A	ENSP00000480593.1:p.Asp2052Asn
ENST00000610817.5:c.7207G>A	ENSP00000480593.2:n.7207G>A
ENST00000673639.2:c.280-2225G>A
ENST00000676696.1:c.7429G>A	ENSP00000503392.1:n.7429G>A
ENST00000678304.1:n.2868G>A
XM_011531127.1:c.7054G>A	XP_011529429.1:p.Asp2352Asn
XM_011531128.1:c.7030G>A	XP_011529430.1:p.Asp2344Asn
XM_011531129.1:c.6976G>A	XP_011529431.1:p.Asp2326Asn
XM_011531130.1:c.6952G>A	XP_011529432.1:p.Asp2318Asn
XM_011531131.1:c.6949G>A	XP_011529433.1:p.Asp2317Asn