Canonical Allele Identifier: CA415192951

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581143G>T (hg19) ; chrX:g.154352775G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352775G>T , CM000685.2:g.154352775G>T	GRCh38
NC_000023.10:g.153581143G>T , CM000685.1:g.153581143G>T	GRCh37
NC_000023.9:g.153234337G>T	NCBI36
NG_011506.1:g.26864C>A
NG_011506.2:g.26864C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6352C>A	ENSP00000353467.4:p.Pro2118Thr
ENST00000369850.10:c.6376C>A MANE Select	ENSP00000358866.3:p.Pro2126Thr
ENST00000369856.8:c.6295C>A	ENSP00000358872.4:p.Pro2099Thr
ENST00000422373.6:c.3161-100C>A	ENSP00000416926.2:n.3161-100C>A
ENST00000610817.5:c.6433C>A	ENSP00000480593.2:n.6433C>A
ENST00000673639.2:c.280-4085C>A
ENST00000676696.1:c.6655C>A	ENSP00000503392.1:n.6655C>A
ENST00000678304.1:n.1555C>A
ENST00000344736.8:c.6256C>A	ENSP00000358863.3:p.Pro2086Thr
ENST00000360319.8:c.6352C>A	ENSP00000353467.4:p.Pro2118Thr
ENST00000369850.7:c.6376C>A	ENSP00000358866.3:p.Pro2126Thr
ENST00000369856.7:c.6295C>A	ENSP00000358872.4:p.Pro2099Thr
ENST00000415241.1:c.578C>A
ENST00000420627.5:c.6332C>A	ENSP00000408921.1:n.6332C>A
ENST00000422373.5:c.6352C>A	ENSP00000416926.1:p.Pro2118Thr
ENST00000444578.1:c.319C>A	ENSP00000397824.1:p.Pro107Thr
ENST00000466325.1:n.591C>A
ENST00000474358.5:n.9C>A
ENST00000490936.5:n.2365C>A
ENST00000498411.1:n.67+42C>A
ENST00000610817.4:c.5844+618C>A	ENSP00000480593.1:n.5844+618C>A
NM_001110556.1:c.6376C>A	NP_001104026.1:p.Pro2126Thr
NM_001456.3:c.6352C>A	NP_001447.2:p.Pro2118Thr
XM_011531127.1:c.6280C>A	XP_011529429.1:p.Pro2094Thr
XM_011531128.1:c.6256C>A	XP_011529430.1:p.Pro2086Thr
XM_011531129.1:c.6202C>A	XP_011529431.1:p.Pro2068Thr
XM_011531130.1:c.6178C>A	XP_011529432.1:p.Pro2060Thr
XM_011531131.1:c.6175C>A	XP_011529433.1:p.Pro2059Thr
NM_001110556.2:c.6376C>A MANE Select	NP_001104026.1:p.Pro2126Thr
NM_001456.4:c.6352C>A	NP_001447.2:p.Pro2118Thr