Canonical Allele Identifier: CA415184913

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153579315C>A (hg19) ; chrX:g.154350947C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350947C>A , CM000685.2:g.154350947C>A	GRCh38
NC_000023.10:g.153579315C>A , CM000685.1:g.153579315C>A	GRCh37
NC_000023.9:g.153232509C>A	NCBI36
NG_011506.1:g.28692G>T
NG_011506.2:g.28692G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7094G>T	ENSP00000353467.4:p.Gly2365Val
ENST00000369850.10:c.7118G>T MANE Select	ENSP00000358866.3:p.Gly2373Val
ENST00000369856.8:c.7037G>T	ENSP00000358872.4:p.Gly2346Val
ENST00000422373.6:c.3899G>T	ENSP00000416926.2:p.Gly1300Val
ENST00000610817.5:c.7175G>T	ENSP00000480593.2:n.7175G>T
ENST00000673639.2:c.280-2257G>T
ENST00000676696.1:c.7397G>T	ENSP00000503392.1:n.7397G>T
ENST00000678304.1:n.2836G>T
ENST00000344736.8:c.6998G>T	ENSP00000358863.3:p.Gly2333Val
ENST00000360319.8:c.7094G>T	ENSP00000353467.4:p.Gly2365Val
ENST00000369850.7:c.7118G>T	ENSP00000358866.3:p.Gly2373Val
ENST00000369856.7:c.7037G>T	ENSP00000358872.4:p.Gly2346Val
ENST00000420627.5:c.7074G>T	ENSP00000408921.1:n.7074G>T
ENST00000422373.5:c.7094G>T	ENSP00000416926.1:p.Gly2365Val
ENST00000490936.5:n.3646G>T
ENST00000498411.1:n.67+1870G>T
ENST00000498491.5:n.159G>T
ENST00000610817.4:c.6122G>T	ENSP00000480593.1:p.Gly2041Val
NM_001110556.1:c.7118G>T	NP_001104026.1:p.Gly2373Val
NM_001456.3:c.7094G>T	NP_001447.2:p.Gly2365Val
XM_011531127.1:c.7022G>T	XP_011529429.1:p.Gly2341Val
XM_011531128.1:c.6998G>T	XP_011529430.1:p.Gly2333Val
XM_011531129.1:c.6944G>T	XP_011529431.1:p.Gly2315Val
XM_011531130.1:c.6920G>T	XP_011529432.1:p.Gly2307Val
XM_011531131.1:c.6917G>T	XP_011529433.1:p.Gly2306Val
NM_001110556.2:c.7118G>T MANE Select	NP_001104026.1:p.Gly2373Val
NM_001456.4:c.7094G>T	NP_001447.2:p.Gly2365Val