Canonical Allele Identifier: CA415184676

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153579282T>A (hg19) ; chrX:g.154350914T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350914T>A , CM000685.2:g.154350914T>A	GRCh38
NC_000023.10:g.153579282T>A , CM000685.1:g.153579282T>A	GRCh37
NC_000023.9:g.153232476T>A	NCBI36
NG_011506.1:g.28725A>T
NG_011506.2:g.28725A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7127A>T	ENSP00000353467.4:p.Asp2376Val
ENST00000369850.10:c.7151A>T MANE Select	ENSP00000358866.3:p.Asp2384Val
ENST00000369856.8:c.7070A>T	ENSP00000358872.4:p.Asp2357Val
ENST00000422373.6:c.3932A>T	ENSP00000416926.2:p.Asp1311Val
ENST00000610817.5:c.7208A>T	ENSP00000480593.2:n.7208A>T
ENST00000673639.2:c.280-2224A>T
ENST00000676696.1:c.7430A>T	ENSP00000503392.1:n.7430A>T
ENST00000678304.1:n.2869A>T
ENST00000344736.8:c.7031A>T	ENSP00000358863.3:p.Asp2344Val
ENST00000360319.8:c.7127A>T	ENSP00000353467.4:p.Asp2376Val
ENST00000369850.7:c.7151A>T	ENSP00000358866.3:p.Asp2384Val
ENST00000369856.7:c.7070A>T	ENSP00000358872.4:p.Asp2357Val
ENST00000420627.5:c.7107A>T	ENSP00000408921.1:n.7107A>T
ENST00000422373.5:c.7127A>T	ENSP00000416926.1:p.Asp2376Val
ENST00000490936.5:n.3679A>T
ENST00000498411.1:n.67+1903A>T
ENST00000498491.5:n.192A>T
ENST00000610817.4:c.6155A>T	ENSP00000480593.1:p.Asp2052Val
NM_001110556.1:c.7151A>T	NP_001104026.1:p.Asp2384Val
NM_001456.3:c.7127A>T	NP_001447.2:p.Asp2376Val
XM_011531127.1:c.7055A>T	XP_011529429.1:p.Asp2352Val
XM_011531128.1:c.7031A>T	XP_011529430.1:p.Asp2344Val
XM_011531129.1:c.6977A>T	XP_011529431.1:p.Asp2326Val
XM_011531130.1:c.6953A>T	XP_011529432.1:p.Asp2318Val
XM_011531131.1:c.6950A>T	XP_011529433.1:p.Asp2317Val
NM_001110556.2:c.7151A>T MANE Select	NP_001104026.1:p.Asp2384Val
NM_001456.4:c.7127A>T	NP_001447.2:p.Asp2376Val