Canonical Allele Identifier: CA415192938

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581142G>T (hg19) ; chrX:g.154352774G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352774G>T , CM000685.2:g.154352774G>T	GRCh38
NC_000023.10:g.153581142G>T , CM000685.1:g.153581142G>T	GRCh37
NC_000023.9:g.153234336G>T	NCBI36
NG_011506.1:g.26865C>A
NG_011506.2:g.26865C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6353C>A	ENSP00000353467.4:p.Pro2118His
ENST00000369850.10:c.6377C>A MANE Select	ENSP00000358866.3:p.Pro2126His
ENST00000369856.8:c.6296C>A	ENSP00000358872.4:p.Pro2099His
ENST00000422373.6:c.3161-99C>A	ENSP00000416926.2:n.3161-99C>A
ENST00000610817.5:c.6434C>A	ENSP00000480593.2:n.6434C>A
ENST00000673639.2:c.280-4084C>A
ENST00000676696.1:c.6656C>A	ENSP00000503392.1:n.6656C>A
ENST00000678304.1:n.1556C>A
ENST00000344736.8:c.6257C>A	ENSP00000358863.3:p.Pro2086His
ENST00000360319.8:c.6353C>A	ENSP00000353467.4:p.Pro2118His
ENST00000369850.7:c.6377C>A	ENSP00000358866.3:p.Pro2126His
ENST00000369856.7:c.6296C>A	ENSP00000358872.4:p.Pro2099His
ENST00000415241.1:c.579C>A
ENST00000420627.5:c.6333C>A	ENSP00000408921.1:n.6333C>A
ENST00000422373.5:c.6353C>A	ENSP00000416926.1:p.Pro2118His
ENST00000444578.1:c.320C>A	ENSP00000397824.1:p.Pro107His
ENST00000466325.1:n.592C>A
ENST00000474358.5:n.10C>A
ENST00000490936.5:n.2366C>A
ENST00000498411.1:n.67+43C>A
ENST00000610817.4:c.5844+619C>A	ENSP00000480593.1:n.5844+619C>A
NM_001110556.1:c.6377C>A	NP_001104026.1:p.Pro2126His
NM_001456.3:c.6353C>A	NP_001447.2:p.Pro2118His
XM_011531127.1:c.6281C>A	XP_011529429.1:p.Pro2094His
XM_011531128.1:c.6257C>A	XP_011529430.1:p.Pro2086His
XM_011531129.1:c.6203C>A	XP_011529431.1:p.Pro2068His
XM_011531130.1:c.6179C>A	XP_011529432.1:p.Pro2060His
XM_011531131.1:c.6176C>A	XP_011529433.1:p.Pro2059His
NM_001110556.2:c.6377C>A MANE Select	NP_001104026.1:p.Pro2126His
NM_001456.4:c.6353C>A	NP_001447.2:p.Pro2118His