Canonical Allele Identifier: CA415193373

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581179A>C (hg19) ; chrX:g.154352811A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352811A>C , CM000685.2:g.154352811A>C	GRCh38
NC_000023.10:g.153581179A>C , CM000685.1:g.153581179A>C	GRCh37
NC_000023.9:g.153234373A>C	NCBI36
NG_011506.1:g.26828T>G
NG_011506.2:g.26828T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.6316T>G	ENSP00000353467.4:p.Tyr2106Asp
ENST00000369850.10:c.6340T>G MANE Select	ENSP00000358866.3:p.Tyr2114Asp
ENST00000369856.8:c.6259T>G	ENSP00000358872.4:p.Tyr2087Asp
ENST00000422373.6:c.3161-136T>G	ENSP00000416926.2:n.3161-136T>G
ENST00000610817.5:c.6397T>G	ENSP00000480593.2:n.6397T>G
ENST00000673639.2:c.280-4121T>G
ENST00000676696.1:c.6619T>G	ENSP00000503392.1:n.6619T>G
ENST00000678304.1:n.1519T>G
ENST00000344736.8:c.6220T>G	ENSP00000358863.3:p.Tyr2074Asp
ENST00000360319.8:c.6316T>G	ENSP00000353467.4:p.Tyr2106Asp
ENST00000369850.7:c.6340T>G	ENSP00000358866.3:p.Tyr2114Asp
ENST00000369856.7:c.6259T>G	ENSP00000358872.4:p.Tyr2087Asp
ENST00000415241.1:c.542T>G
ENST00000420627.5:c.6296T>G	ENSP00000408921.1:n.6296T>G
ENST00000422373.5:c.6316T>G	ENSP00000416926.1:p.Tyr2106Asp
ENST00000444578.1:c.283T>G	ENSP00000397824.1:p.Tyr95Asp
ENST00000466325.1:n.555T>G
ENST00000490936.5:n.2329T>G
ENST00000498411.1:n.67+6T>G
ENST00000610817.4:c.5844+582T>G	ENSP00000480593.1:n.5844+582T>G
NM_001110556.1:c.6340T>G	NP_001104026.1:p.Tyr2114Asp
NM_001456.3:c.6316T>G	NP_001447.2:p.Tyr2106Asp
XM_011531127.1:c.6244T>G	XP_011529429.1:p.Tyr2082Asp
XM_011531128.1:c.6220T>G	XP_011529430.1:p.Tyr2074Asp
XM_011531129.1:c.6166T>G	XP_011529431.1:p.Tyr2056Asp
XM_011531130.1:c.6142T>G	XP_011529432.1:p.Tyr2048Asp
XM_011531131.1:c.6139T>G	XP_011529433.1:p.Tyr2047Asp
NM_001110556.2:c.6340T>G MANE Select	NP_001104026.1:p.Tyr2114Asp
NM_001456.4:c.6316T>G	NP_001447.2:p.Tyr2106Asp