Canonical Allele Identifier: CA519706168

Gene: FLNA

Linked Data

• dbSNP Id: rs1569551482
• MyVariant Identifiers: chrX:g.153581409G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353041G>T , CM000685.2:g.154353041G>T	GRCh38
NC_000023.10:g.153581409G>T , CM000685.1:g.153581409G>T	GRCh37
NC_000023.9:g.153234603G>T	NCBI36
NG_011506.1:g.26598C>A
NG_011506.2:g.26598C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6162C>A	ENSP00000353467.4:p.Thr2054=
ENST00000369850.10:c.6186C>A MANE Select	ENSP00000358866.3:p.Thr2062=
ENST00000369856.8:c.6105C>A	ENSP00000358872.4:p.Thr2035=
ENST00000422373.6:c.3161-366C>A	ENSP00000416926.2:n.3161-366C>A
ENST00000610817.5:c.6243C>A	ENSP00000480593.2:n.6243C>A
ENST00000673639.2:c.280-4351C>A
ENST00000676696.1:c.6465C>A	ENSP00000503392.1:n.6465C>A
ENST00000678304.1:n.1365C>A
ENST00000344736.8:c.6066C>A	ENSP00000358863.3:p.Thr2022=
ENST00000360319.8:c.6162C>A	ENSP00000353467.4:p.Thr2054=
ENST00000369850.7:c.6186C>A	ENSP00000358866.3:p.Thr2062=
ENST00000369856.7:c.6105C>A	ENSP00000358872.4:p.Thr2035=
ENST00000415241.1:c.388C>A
ENST00000420627.5:c.6142C>A	ENSP00000408921.1:n.6142C>A
ENST00000422373.5:c.6162C>A	ENSP00000416926.1:p.Thr2054=
ENST00000444578.1:c.129C>A	ENSP00000397824.1:p.Thr43=
ENST00000466325.1:n.325C>A
ENST00000490936.5:n.2175C>A
ENST00000610817.4:c.5844+352C>A	ENSP00000480593.1:n.5844+352C>A
NM_001110556.1:c.6186C>A	NP_001104026.1:p.Thr2062=
NM_001456.3:c.6162C>A	NP_001447.2:p.Thr2054=
XM_011531127.1:c.6090C>A	XP_011529429.1:p.Thr2030=
XM_011531128.1:c.6066C>A	XP_011529430.1:p.Thr2022=
XM_011531129.1:c.6012C>A	XP_011529431.1:p.Thr2004=
XM_011531130.1:c.5988C>A	XP_011529432.1:p.Thr1996=
XM_011531131.1:c.5985C>A	XP_011529433.1:p.Thr1995=
NM_001110556.2:c.6186C>A MANE Select	NP_001104026.1:p.Thr2062=
NM_001456.4:c.6162C>A	NP_001447.2:p.Thr2054=