Canonical Allele Identifier: CA519276778

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153587401T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154359033T>A , CM000685.2:g.154359033T>A	GRCh38
NC_000023.10:g.153587401T>A , CM000685.1:g.153587401T>A	GRCh37
NC_000023.9:g.153240595T>A	NCBI36
NG_011506.1:g.20606A>T
NG_011506.2:g.20606A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.4425A>T	ENSP00000353467.4:p.Thr1475=
ENST00000369850.10:c.4425A>T MANE Select	ENSP00000358866.3:p.Thr1475=
ENST00000369856.8:c.4344A>T	ENSP00000358872.4:p.Thr1448=
ENST00000422373.6:c.3160+2322A>T	ENSP00000416926.2:n.3160+2322A>T
ENST00000610817.5:c.4482A>T	ENSP00000480593.2:n.4482A>T
ENST00000673639.2:c.279+6403A>T
ENST00000676696.1:c.4704A>T	ENSP00000503392.1:n.4704A>T
ENST00000678304.1:n.148+56A>T
ENST00000344736.8:c.4425A>T	ENSP00000358863.3:p.Thr1475=
ENST00000360319.8:c.4425A>T	ENSP00000353467.4:p.Thr1475=
ENST00000369850.7:c.4425A>T	ENSP00000358866.3:p.Thr1475=
ENST00000369856.7:c.4344A>T	ENSP00000358872.4:p.Thr1448=
ENST00000420627.5:c.4381A>T	ENSP00000408921.1:n.4381A>T
ENST00000422373.5:c.4425A>T	ENSP00000416926.1:p.Thr1475=
ENST00000490936.5:n.438A>T
ENST00000610817.4:c.4344A>T	ENSP00000480593.1:p.Thr1448=
NM_001110556.1:c.4425A>T	NP_001104026.1:p.Thr1475=
NM_001456.3:c.4425A>T	NP_001447.2:p.Thr1475=
XM_011531127.1:c.4425A>T	XP_011529429.1:p.Thr1475=
XM_011531128.1:c.4425A>T	XP_011529430.1:p.Thr1475=
XM_011531129.1:c.4425A>T	XP_011529431.1:p.Thr1475=
XM_011531130.1:c.4425A>T	XP_011529432.1:p.Thr1475=
XM_011531131.1:c.4224A>T	XP_011529433.1:p.Thr1408=
NM_001110556.2:c.4425A>T MANE Select	NP_001104026.1:p.Thr1475=
NM_001456.4:c.4425A>T	NP_001447.2:p.Thr1475=