Canonical Allele Identifier: CA415197122

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581687T>C (hg19) ; chrX:g.154353319T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353319T>C , CM000685.2:g.154353319T>C	GRCh38
NC_000023.10:g.153581687T>C , CM000685.1:g.153581687T>C	GRCh37
NC_000023.9:g.153234881T>C	NCBI36
NG_011506.1:g.26320A>G
NG_011506.2:g.26320A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5975A>G	ENSP00000353467.4:p.Lys1992Arg
ENST00000369850.10:c.5999A>G MANE Select	ENSP00000358866.3:p.Lys2000Arg
ENST00000369856.8:c.5918A>G	ENSP00000358872.4:p.Lys1973Arg
ENST00000422373.6:c.3161-644A>G	ENSP00000416926.2:n.3161-644A>G
ENST00000610817.5:c.6056A>G	ENSP00000480593.2:n.6056A>G
ENST00000673639.2:c.280-4629A>G
ENST00000676696.1:c.6278A>G	ENSP00000503392.1:n.6278A>G
ENST00000678304.1:n.1178A>G
ENST00000344736.8:c.5879A>G	ENSP00000358863.3:p.Lys1960Arg
ENST00000360319.8:c.5975A>G	ENSP00000353467.4:p.Lys1992Arg
ENST00000369850.7:c.5999A>G	ENSP00000358866.3:p.Lys2000Arg
ENST00000369856.7:c.5918A>G	ENSP00000358872.4:p.Lys1973Arg
ENST00000415241.1:c.184A>G
ENST00000420627.5:c.5955A>G	ENSP00000408921.1:n.5955A>G
ENST00000422373.5:c.5975A>G	ENSP00000416926.1:p.Lys1992Arg
ENST00000438732.2:c.673A>G
ENST00000466325.1:n.138A>G
ENST00000490936.5:n.1988A>G
ENST00000610817.4:c.5844+74A>G	ENSP00000480593.1:n.5844+74A>G
NM_001110556.1:c.5999A>G	NP_001104026.1:p.Lys2000Arg
NM_001456.3:c.5975A>G	NP_001447.2:p.Lys1992Arg
XM_011531127.1:c.5903A>G	XP_011529429.1:p.Lys1968Arg
XM_011531128.1:c.5879A>G	XP_011529430.1:p.Lys1960Arg
XM_011531129.1:c.5825A>G	XP_011529431.1:p.Lys1942Arg
XM_011531130.1:c.5801A>G	XP_011529432.1:p.Lys1934Arg
XM_011531131.1:c.5798A>G	XP_011529433.1:p.Lys1933Arg
NM_001110556.2:c.5999A>G MANE Select	NP_001104026.1:p.Lys2000Arg
NM_001456.4:c.5975A>G	NP_001447.2:p.Lys1992Arg