Canonical Allele Identifier: CA519706542

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581009G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352641G>A , CM000685.2:g.154352641G>A	GRCh38
NC_000023.10:g.153581009G>A , CM000685.1:g.153581009G>A	GRCh37
NC_000023.9:g.153234203G>A	NCBI36
NG_011506.1:g.26998C>T
NG_011506.2:g.26998C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6390C>T	ENSP00000353467.4:p.Gly2130=
ENST00000369850.10:c.6414C>T MANE Select	ENSP00000358866.3:p.Gly2138=
ENST00000369856.8:c.6333C>T	ENSP00000358872.4:p.Gly2111=
ENST00000422373.6:c.3195C>T	ENSP00000416926.2:p.Gly1065=
ENST00000610817.5:c.6471C>T	ENSP00000480593.2:n.6471C>T
ENST00000673639.2:c.280-3951C>T
ENST00000676696.1:c.6693C>T	ENSP00000503392.1:n.6693C>T
ENST00000678304.1:n.1593C>T
ENST00000344736.8:c.6294C>T	ENSP00000358863.3:p.Gly2098=
ENST00000360319.8:c.6390C>T	ENSP00000353467.4:p.Gly2130=
ENST00000369850.7:c.6414C>T	ENSP00000358866.3:p.Gly2138=
ENST00000369856.7:c.6333C>T	ENSP00000358872.4:p.Gly2111=
ENST00000415241.1:c.616C>T
ENST00000420627.5:c.6370C>T	ENSP00000408921.1:n.6370C>T
ENST00000422373.5:c.6390C>T	ENSP00000416926.1:p.Gly2130=
ENST00000444578.1:c.322+131C>T	ENSP00000397824.1:n.322+131C>T
ENST00000466325.1:n.725C>T
ENST00000474358.5:n.47C>T
ENST00000490936.5:n.2403C>T
ENST00000498411.1:n.67+176C>T
ENST00000610817.4:c.5845-691C>T	ENSP00000480593.1:n.5845-691C>T
NM_001110556.1:c.6414C>T	NP_001104026.1:p.Gly2138=
NM_001456.3:c.6390C>T	NP_001447.2:p.Gly2130=
XM_011531127.1:c.6318C>T	XP_011529429.1:p.Gly2106=
XM_011531128.1:c.6294C>T	XP_011529430.1:p.Gly2098=
XM_011531129.1:c.6240C>T	XP_011529431.1:p.Gly2080=
XM_011531130.1:c.6216C>T	XP_011529432.1:p.Gly2072=
XM_011531131.1:c.6213C>T	XP_011529433.1:p.Gly2071=
NM_001110556.2:c.6414C>T MANE Select	NP_001104026.1:p.Gly2138=
NM_001456.4:c.6390C>T	NP_001447.2:p.Gly2130=