Canonical Allele Identifier: CA415193027

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581149G>C (hg19) ; chrX:g.154352781G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352781G>C , CM000685.2:g.154352781G>C	GRCh38
NC_000023.10:g.153581149G>C , CM000685.1:g.153581149G>C	GRCh37
NC_000023.9:g.153234343G>C	NCBI36
NG_011506.1:g.26858C>G
NG_011506.2:g.26858C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6346C>G	ENSP00000353467.4:p.His2116Asp
ENST00000369850.10:c.6370C>G MANE Select	ENSP00000358866.3:p.His2124Asp
ENST00000369856.8:c.6289C>G	ENSP00000358872.4:p.His2097Asp
ENST00000422373.6:c.3161-106C>G	ENSP00000416926.2:n.3161-106C>G
ENST00000610817.5:c.6427C>G	ENSP00000480593.2:n.6427C>G
ENST00000673639.2:c.280-4091C>G
ENST00000676696.1:c.6649C>G	ENSP00000503392.1:n.6649C>G
ENST00000678304.1:n.1549C>G
ENST00000344736.8:c.6250C>G	ENSP00000358863.3:p.His2084Asp
ENST00000360319.8:c.6346C>G	ENSP00000353467.4:p.His2116Asp
ENST00000369850.7:c.6370C>G	ENSP00000358866.3:p.His2124Asp
ENST00000369856.7:c.6289C>G	ENSP00000358872.4:p.His2097Asp
ENST00000415241.1:c.572C>G
ENST00000420627.5:c.6326C>G	ENSP00000408921.1:n.6326C>G
ENST00000422373.5:c.6346C>G	ENSP00000416926.1:p.His2116Asp
ENST00000444578.1:c.313C>G	ENSP00000397824.1:p.His105Asp
ENST00000466325.1:n.585C>G
ENST00000474358.5:n.3C>G
ENST00000490936.5:n.2359C>G
ENST00000498411.1:n.67+36C>G
ENST00000610817.4:c.5844+612C>G	ENSP00000480593.1:n.5844+612C>G
NM_001110556.1:c.6370C>G	NP_001104026.1:p.His2124Asp
NM_001456.3:c.6346C>G	NP_001447.2:p.His2116Asp
XM_011531127.1:c.6274C>G	XP_011529429.1:p.His2092Asp
XM_011531128.1:c.6250C>G	XP_011529430.1:p.His2084Asp
XM_011531129.1:c.6196C>G	XP_011529431.1:p.His2066Asp
XM_011531130.1:c.6172C>G	XP_011529432.1:p.His2058Asp
XM_011531131.1:c.6169C>G	XP_011529433.1:p.His2057Asp
NM_001110556.2:c.6370C>G MANE Select	NP_001104026.1:p.His2124Asp
NM_001456.4:c.6346C>G	NP_001447.2:p.His2116Asp