Canonical Allele Identifier: CA519276504

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153579293G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350925G>A , CM000685.2:g.154350925G>A	GRCh38
NC_000023.10:g.153579293G>A , CM000685.1:g.153579293G>A	GRCh37
NC_000023.9:g.153232487G>A	NCBI36
NG_011506.1:g.28714C>T
NG_011506.2:g.28714C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7116C>T	ENSP00000353467.4:p.Val2372=
ENST00000369850.10:c.7140C>T MANE Select	ENSP00000358866.3:p.Val2380=
ENST00000369856.8:c.7059C>T	ENSP00000358872.4:p.Val2353=
ENST00000422373.6:c.3921C>T	ENSP00000416926.2:p.Val1307=
ENST00000610817.5:c.7197C>T	ENSP00000480593.2:n.7197C>T
ENST00000673639.2:c.280-2235C>T
ENST00000676696.1:c.7419C>T	ENSP00000503392.1:n.7419C>T
ENST00000678304.1:n.2858C>T
ENST00000344736.8:c.7020C>T	ENSP00000358863.3:p.Val2340=
ENST00000360319.8:c.7116C>T	ENSP00000353467.4:p.Val2372=
ENST00000369850.7:c.7140C>T	ENSP00000358866.3:p.Val2380=
ENST00000369856.7:c.7059C>T	ENSP00000358872.4:p.Val2353=
ENST00000420627.5:c.7096C>T	ENSP00000408921.1:n.7096C>T
ENST00000422373.5:c.7116C>T	ENSP00000416926.1:p.Val2372=
ENST00000490936.5:n.3668C>T
ENST00000498411.1:n.67+1892C>T
ENST00000498491.5:n.181C>T
ENST00000610817.4:c.6144C>T	ENSP00000480593.1:p.Val2048=
NM_001110556.1:c.7140C>T	NP_001104026.1:p.Val2380=
NM_001456.3:c.7116C>T	NP_001447.2:p.Val2372=
XM_011531127.1:c.7044C>T	XP_011529429.1:p.Val2348=
XM_011531128.1:c.7020C>T	XP_011529430.1:p.Val2340=
XM_011531129.1:c.6966C>T	XP_011529431.1:p.Val2322=
XM_011531130.1:c.6942C>T	XP_011529432.1:p.Val2314=
XM_011531131.1:c.6939C>T	XP_011529433.1:p.Val2313=
NM_001110556.2:c.7140C>T MANE Select	NP_001104026.1:p.Val2380=
NM_001456.4:c.7116C>T	NP_001447.2:p.Val2372=