Canonical Allele Identifier: CA519706860

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581683C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353315C>T , CM000685.2:g.154353315C>T	GRCh38
NC_000023.10:g.153581683C>T , CM000685.1:g.153581683C>T	GRCh37
NC_000023.9:g.153234877C>T	NCBI36
NG_011506.1:g.26324G>A
NG_011506.2:g.26324G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5979G>A	ENSP00000353467.4:p.Arg1993=
ENST00000369850.10:c.6003G>A MANE Select	ENSP00000358866.3:p.Arg2001=
ENST00000369856.8:c.5922G>A	ENSP00000358872.4:p.Arg1974=
ENST00000422373.6:c.3161-640G>A	ENSP00000416926.2:n.3161-640G>A
ENST00000610817.5:c.6060G>A	ENSP00000480593.2:n.6060G>A
ENST00000673639.2:c.280-4625G>A
ENST00000676696.1:c.6282G>A	ENSP00000503392.1:n.6282G>A
ENST00000678304.1:n.1182G>A
ENST00000344736.8:c.5883G>A	ENSP00000358863.3:p.Arg1961=
ENST00000360319.8:c.5979G>A	ENSP00000353467.4:p.Arg1993=
ENST00000369850.7:c.6003G>A	ENSP00000358866.3:p.Arg2001=
ENST00000369856.7:c.5922G>A	ENSP00000358872.4:p.Arg1974=
ENST00000415241.1:c.188G>A
ENST00000420627.5:c.5959G>A	ENSP00000408921.1:n.5959G>A
ENST00000422373.5:c.5979G>A	ENSP00000416926.1:p.Arg1993=
ENST00000438732.2:c.677G>A
ENST00000466325.1:n.142G>A
ENST00000490936.5:n.1992G>A
ENST00000610817.4:c.5844+78G>A	ENSP00000480593.1:n.5844+78G>A
NM_001110556.1:c.6003G>A	NP_001104026.1:p.Arg2001=
NM_001456.3:c.5979G>A	NP_001447.2:p.Arg1993=
XM_011531127.1:c.5907G>A	XP_011529429.1:p.Arg1969=
XM_011531128.1:c.5883G>A	XP_011529430.1:p.Arg1961=
XM_011531129.1:c.5829G>A	XP_011529431.1:p.Arg1943=
XM_011531130.1:c.5805G>A	XP_011529432.1:p.Arg1935=
XM_011531131.1:c.5802G>A	XP_011529433.1:p.Arg1934=
NM_001110556.2:c.6003G>A MANE Select	NP_001104026.1:p.Arg2001=
NM_001456.4:c.5979G>A	NP_001447.2:p.Arg1993=