Canonical Allele Identifier: CA415197237

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581699G>T (hg19) ; chrX:g.154353331G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353331G>T , CM000685.2:g.154353331G>T	GRCh38
NC_000023.10:g.153581699G>T , CM000685.1:g.153581699G>T	GRCh37
NC_000023.9:g.153234893G>T	NCBI36
NG_011506.1:g.26308C>A
NG_011506.2:g.26308C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5963C>A	ENSP00000353467.4:p.Pro1988His
ENST00000369850.10:c.5987C>A MANE Select	ENSP00000358866.3:p.Pro1996His
ENST00000369856.8:c.5906C>A	ENSP00000358872.4:p.Pro1969His
ENST00000422373.6:c.3161-656C>A	ENSP00000416926.2:n.3161-656C>A
ENST00000610817.5:c.6044C>A	ENSP00000480593.2:n.6044C>A
ENST00000673639.2:c.280-4641C>A
ENST00000676696.1:c.6266C>A	ENSP00000503392.1:n.6266C>A
ENST00000678304.1:n.1166C>A
ENST00000344736.8:c.5867C>A	ENSP00000358863.3:p.Pro1956His
ENST00000360319.8:c.5963C>A	ENSP00000353467.4:p.Pro1988His
ENST00000369850.7:c.5987C>A	ENSP00000358866.3:p.Pro1996His
ENST00000369856.7:c.5906C>A	ENSP00000358872.4:p.Pro1969His
ENST00000415241.1:c.172C>A
ENST00000420627.5:c.5943C>A	ENSP00000408921.1:n.5943C>A
ENST00000422373.5:c.5963C>A	ENSP00000416926.1:p.Pro1988His
ENST00000438732.2:c.661C>A
ENST00000466325.1:n.126C>A
ENST00000490936.5:n.1976C>A
ENST00000610817.4:c.5844+62C>A	ENSP00000480593.1:n.5844+62C>A
NM_001110556.1:c.5987C>A	NP_001104026.1:p.Pro1996His
NM_001456.3:c.5963C>A	NP_001447.2:p.Pro1988His
XM_011531127.1:c.5891C>A	XP_011529429.1:p.Pro1964His
XM_011531128.1:c.5867C>A	XP_011529430.1:p.Pro1956His
XM_011531129.1:c.5813C>A	XP_011529431.1:p.Pro1938His
XM_011531130.1:c.5789C>A	XP_011529432.1:p.Pro1930His
XM_011531131.1:c.5786C>A	XP_011529433.1:p.Pro1929His
NM_001110556.2:c.5987C>A MANE Select	NP_001104026.1:p.Pro1996His
NM_001456.4:c.5963C>A	NP_001447.2:p.Pro1988His