Canonical Allele Identifier: CA415194726

Gene: FLNA

Linked Data

• gnomAD v4: X-154352924-C-T
• MyVariant Identifiers: chrX:g.153581292C>T (hg19) ; chrX:g.154352924C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352924C>T , CM000685.2:g.154352924C>T	GRCh38
NC_000023.10:g.153581292C>T , CM000685.1:g.153581292C>T	GRCh37
NC_000023.9:g.153234486C>T	NCBI36
NG_011506.1:g.26715G>A
NG_011506.2:g.26715G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6203G>A	ENSP00000353467.4:p.Gly2068Asp
ENST00000369850.10:c.6227G>A MANE Select	ENSP00000358866.3:p.Gly2076Asp
ENST00000369856.8:c.6146G>A	ENSP00000358872.4:p.Gly2049Asp
ENST00000422373.6:c.3161-249G>A	ENSP00000416926.2:n.3161-249G>A
ENST00000610817.5:c.6284G>A	ENSP00000480593.2:n.6284G>A
ENST00000673639.2:c.280-4234G>A
ENST00000676696.1:c.6506G>A	ENSP00000503392.1:n.6506G>A
ENST00000678304.1:n.1406G>A
ENST00000344736.8:c.6107G>A	ENSP00000358863.3:p.Gly2036Asp
ENST00000360319.8:c.6203G>A	ENSP00000353467.4:p.Gly2068Asp
ENST00000369850.7:c.6227G>A	ENSP00000358866.3:p.Gly2076Asp
ENST00000369856.7:c.6146G>A	ENSP00000358872.4:p.Gly2049Asp
ENST00000415241.1:c.429G>A
ENST00000420627.5:c.6183G>A	ENSP00000408921.1:n.6183G>A
ENST00000422373.5:c.6203G>A	ENSP00000416926.1:p.Gly2068Asp
ENST00000444578.1:c.170G>A	ENSP00000397824.1:p.Gly57Asp
ENST00000466325.1:n.442G>A
ENST00000490936.5:n.2216G>A
ENST00000610817.4:c.5844+469G>A	ENSP00000480593.1:n.5844+469G>A
NM_001110556.1:c.6227G>A	NP_001104026.1:p.Gly2076Asp
NM_001456.3:c.6203G>A	NP_001447.2:p.Gly2068Asp
XM_011531127.1:c.6131G>A	XP_011529429.1:p.Gly2044Asp
XM_011531128.1:c.6107G>A	XP_011529430.1:p.Gly2036Asp
XM_011531129.1:c.6053G>A	XP_011529431.1:p.Gly2018Asp
XM_011531130.1:c.6029G>A	XP_011529432.1:p.Gly2010Asp
XM_011531131.1:c.6026G>A	XP_011529433.1:p.Gly2009Asp
NM_001110556.2:c.6227G>A MANE Select	NP_001104026.1:p.Gly2076Asp
NM_001456.4:c.6203G>A	NP_001447.2:p.Gly2068Asp