Canonical Allele Identifier: CA415197220

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581697A>T (hg19) ; chrX:g.154353329A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353329A>T , CM000685.2:g.154353329A>T	GRCh38
NC_000023.10:g.153581697A>T , CM000685.1:g.153581697A>T	GRCh37
NC_000023.9:g.153234891A>T	NCBI36
NG_011506.1:g.26310T>A
NG_011506.2:g.26310T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5965T>A	ENSP00000353467.4:p.Cys1989Ser
ENST00000369850.10:c.5989T>A MANE Select	ENSP00000358866.3:p.Cys1997Ser
ENST00000369856.8:c.5908T>A	ENSP00000358872.4:p.Cys1970Ser
ENST00000422373.6:c.3161-654T>A	ENSP00000416926.2:n.3161-654T>A
ENST00000610817.5:c.6046T>A	ENSP00000480593.2:n.6046T>A
ENST00000673639.2:c.280-4639T>A
ENST00000676696.1:c.6268T>A	ENSP00000503392.1:n.6268T>A
ENST00000678304.1:n.1168T>A
ENST00000344736.8:c.5869T>A	ENSP00000358863.3:p.Cys1957Ser
ENST00000360319.8:c.5965T>A	ENSP00000353467.4:p.Cys1989Ser
ENST00000369850.7:c.5989T>A	ENSP00000358866.3:p.Cys1997Ser
ENST00000369856.7:c.5908T>A	ENSP00000358872.4:p.Cys1970Ser
ENST00000415241.1:c.174T>A
ENST00000420627.5:c.5945T>A	ENSP00000408921.1:n.5945T>A
ENST00000422373.5:c.5965T>A	ENSP00000416926.1:p.Cys1989Ser
ENST00000438732.2:c.663T>A
ENST00000466325.1:n.128T>A
ENST00000490936.5:n.1978T>A
ENST00000610817.4:c.5844+64T>A	ENSP00000480593.1:n.5844+64T>A
NM_001110556.1:c.5989T>A	NP_001104026.1:p.Cys1997Ser
NM_001456.3:c.5965T>A	NP_001447.2:p.Cys1989Ser
XM_011531127.1:c.5893T>A	XP_011529429.1:p.Cys1965Ser
XM_011531128.1:c.5869T>A	XP_011529430.1:p.Cys1957Ser
XM_011531129.1:c.5815T>A	XP_011529431.1:p.Cys1939Ser
XM_011531130.1:c.5791T>A	XP_011529432.1:p.Cys1931Ser
XM_011531131.1:c.5788T>A	XP_011529433.1:p.Cys1930Ser
NM_001110556.2:c.5989T>A MANE Select	NP_001104026.1:p.Cys1997Ser
NM_001456.4:c.5965T>A	NP_001447.2:p.Cys1989Ser