Canonical Allele Identifier: CA519706189

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581439G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353071G>T , CM000685.2:g.154353071G>T	GRCh38
NC_000023.10:g.153581439G>T , CM000685.1:g.153581439G>T	GRCh37
NC_000023.9:g.153234633G>T	NCBI36
NG_011506.1:g.26568C>A
NG_011506.2:g.26568C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6132C>A	ENSP00000353467.4:p.Val2044=
ENST00000369850.10:c.6156C>A MANE Select	ENSP00000358866.3:p.Val2052=
ENST00000369856.8:c.6075C>A	ENSP00000358872.4:p.Val2025=
ENST00000422373.6:c.3161-396C>A	ENSP00000416926.2:n.3161-396C>A
ENST00000610817.5:c.6213C>A	ENSP00000480593.2:n.6213C>A
ENST00000673639.2:c.280-4381C>A
ENST00000676696.1:c.6435C>A	ENSP00000503392.1:n.6435C>A
ENST00000678304.1:n.1335C>A
ENST00000344736.8:c.6036C>A	ENSP00000358863.3:p.Val2012=
ENST00000360319.8:c.6132C>A	ENSP00000353467.4:p.Val2044=
ENST00000369850.7:c.6156C>A	ENSP00000358866.3:p.Val2052=
ENST00000369856.7:c.6075C>A	ENSP00000358872.4:p.Val2025=
ENST00000415241.1:c.358C>A
ENST00000420627.5:c.6112C>A	ENSP00000408921.1:n.6112C>A
ENST00000422373.5:c.6132C>A	ENSP00000416926.1:p.Val2044=
ENST00000444578.1:c.99C>A	ENSP00000397824.1:p.Val33=
ENST00000466325.1:n.295C>A
ENST00000490936.5:n.2145C>A
ENST00000610817.4:c.5844+322C>A	ENSP00000480593.1:n.5844+322C>A
NM_001110556.1:c.6156C>A	NP_001104026.1:p.Val2052=
NM_001456.3:c.6132C>A	NP_001447.2:p.Val2044=
XM_011531127.1:c.6060C>A	XP_011529429.1:p.Val2020=
XM_011531128.1:c.6036C>A	XP_011529430.1:p.Val2012=
XM_011531129.1:c.5982C>A	XP_011529431.1:p.Val1994=
XM_011531130.1:c.5958C>A	XP_011529432.1:p.Val1986=
XM_011531131.1:c.5955C>A	XP_011529433.1:p.Val1985=
NM_001110556.2:c.6156C>A MANE Select	NP_001104026.1:p.Val2052=
NM_001456.4:c.6132C>A	NP_001447.2:p.Val2044=