Canonical Allele Identifier: CA519276789

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153587419C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154359051C>T , CM000685.2:g.154359051C>T	GRCh38
NC_000023.10:g.153587419C>T , CM000685.1:g.153587419C>T	GRCh37
NC_000023.9:g.153240613C>T	NCBI36
NG_011506.1:g.20588G>A
NG_011506.2:g.20588G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.4407G>A	ENSP00000353467.4:p.Gln1469=
ENST00000369850.10:c.4407G>A MANE Select	ENSP00000358866.3:p.Gln1469=
ENST00000369856.8:c.4326G>A	ENSP00000358872.4:p.Gln1442=
ENST00000422373.6:c.3160+2304G>A	ENSP00000416926.2:n.3160+2304G>A
ENST00000610817.5:c.4464G>A	ENSP00000480593.2:n.4464G>A
ENST00000673639.2:c.279+6385G>A
ENST00000676696.1:c.4686G>A	ENSP00000503392.1:n.4686G>A
ENST00000678304.1:n.148+38G>A
ENST00000344736.8:c.4407G>A	ENSP00000358863.3:p.Gln1469=
ENST00000360319.8:c.4407G>A	ENSP00000353467.4:p.Gln1469=
ENST00000369850.7:c.4407G>A	ENSP00000358866.3:p.Gln1469=
ENST00000369856.7:c.4326G>A	ENSP00000358872.4:p.Gln1442=
ENST00000420627.5:c.4363G>A	ENSP00000408921.1:n.4363G>A
ENST00000422373.5:c.4407G>A	ENSP00000416926.1:p.Gln1469=
ENST00000490936.5:n.420G>A
ENST00000610817.4:c.4326G>A	ENSP00000480593.1:p.Gln1442=
NM_001110556.1:c.4407G>A	NP_001104026.1:p.Gln1469=
NM_001456.3:c.4407G>A	NP_001447.2:p.Gln1469=
XM_011531127.1:c.4407G>A	XP_011529429.1:p.Gln1469=
XM_011531128.1:c.4407G>A	XP_011529430.1:p.Gln1469=
XM_011531129.1:c.4407G>A	XP_011529431.1:p.Gln1469=
XM_011531130.1:c.4407G>A	XP_011529432.1:p.Gln1469=
XM_011531131.1:c.4206G>A	XP_011529433.1:p.Gln1402=
NM_001110556.2:c.4407G>A MANE Select	NP_001104026.1:p.Gln1469=
NM_001456.4:c.4407G>A	NP_001447.2:p.Gln1469=