Canonical Allele Identifier: CA415197386

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581715A>T (hg19) ; chrX:g.154353347A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353347A>T , CM000685.2:g.154353347A>T	GRCh38
NC_000023.10:g.153581715A>T , CM000685.1:g.153581715A>T	GRCh37
NC_000023.9:g.153234909A>T	NCBI36
NG_011506.1:g.26292T>A
NG_011506.2:g.26292T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5947T>A	ENSP00000353467.4:p.Ser1983Thr
ENST00000369850.10:c.5971T>A MANE Select	ENSP00000358866.3:p.Ser1991Thr
ENST00000369856.8:c.5890T>A	ENSP00000358872.4:p.Ser1964Thr
ENST00000422373.6:c.3161-672T>A	ENSP00000416926.2:n.3161-672T>A
ENST00000610817.5:c.6028T>A	ENSP00000480593.2:n.6028T>A
ENST00000673639.2:c.280-4657T>A
ENST00000676696.1:c.6250T>A	ENSP00000503392.1:n.6250T>A
ENST00000678304.1:n.1150T>A
ENST00000344736.8:c.5851T>A	ENSP00000358863.3:p.Ser1951Thr
ENST00000360319.8:c.5947T>A	ENSP00000353467.4:p.Ser1983Thr
ENST00000369850.7:c.5971T>A	ENSP00000358866.3:p.Ser1991Thr
ENST00000369856.7:c.5890T>A	ENSP00000358872.4:p.Ser1964Thr
ENST00000415241.1:c.156T>A
ENST00000420627.5:c.5927T>A	ENSP00000408921.1:n.5927T>A
ENST00000422373.5:c.5947T>A	ENSP00000416926.1:p.Ser1983Thr
ENST00000438732.2:c.645T>A
ENST00000466325.1:n.110T>A
ENST00000490936.5:n.1960T>A
ENST00000610817.4:c.5844+46T>A	ENSP00000480593.1:n.5844+46T>A
NM_001110556.1:c.5971T>A	NP_001104026.1:p.Ser1991Thr
NM_001456.3:c.5947T>A	NP_001447.2:p.Ser1983Thr
XM_011531127.1:c.5875T>A	XP_011529429.1:p.Ser1959Thr
XM_011531128.1:c.5851T>A	XP_011529430.1:p.Ser1951Thr
XM_011531129.1:c.5797T>A	XP_011529431.1:p.Ser1933Thr
XM_011531130.1:c.5773T>A	XP_011529432.1:p.Ser1925Thr
XM_011531131.1:c.5770T>A	XP_011529433.1:p.Ser1924Thr
NM_001110556.2:c.5971T>A MANE Select	NP_001104026.1:p.Ser1991Thr
NM_001456.4:c.5947T>A	NP_001447.2:p.Ser1983Thr