Canonical Allele Identifier: CA415196757

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581570T>C (hg19) ; chrX:g.154353202T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353202T>C , CM000685.2:g.154353202T>C	GRCh38
NC_000023.10:g.153581570T>C , CM000685.1:g.153581570T>C	GRCh37
NC_000023.9:g.153234764T>C	NCBI36
NG_011506.1:g.26437A>G
NG_011506.2:g.26437A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6001A>G	ENSP00000353467.4:p.Ile2001Val
ENST00000369850.10:c.6025A>G MANE Select	ENSP00000358866.3:p.Ile2009Val
ENST00000369856.8:c.5944A>G	ENSP00000358872.4:p.Ile1982Val
ENST00000422373.6:c.3161-527A>G	ENSP00000416926.2:n.3161-527A>G
ENST00000610817.5:c.6082A>G	ENSP00000480593.2:n.6082A>G
ENST00000673639.2:c.280-4512A>G
ENST00000676696.1:c.6304A>G	ENSP00000503392.1:n.6304A>G
ENST00000678304.1:n.1204A>G
ENST00000344736.8:c.5905A>G	ENSP00000358863.3:p.Ile1969Val
ENST00000360319.8:c.6001A>G	ENSP00000353467.4:p.Ile2001Val
ENST00000369850.7:c.6025A>G	ENSP00000358866.3:p.Ile2009Val
ENST00000369856.7:c.5944A>G	ENSP00000358872.4:p.Ile1982Val
ENST00000415241.1:c.227A>G
ENST00000420627.5:c.5981A>G	ENSP00000408921.1:n.5981A>G
ENST00000422373.5:c.6001A>G	ENSP00000416926.1:p.Ile2001Val
ENST00000466325.1:n.164A>G
ENST00000490936.5:n.2014A>G
ENST00000610817.4:c.5844+191A>G	ENSP00000480593.1:n.5844+191A>G
NM_001110556.1:c.6025A>G	NP_001104026.1:p.Ile2009Val
NM_001456.3:c.6001A>G	NP_001447.2:p.Ile2001Val
XM_011531127.1:c.5929A>G	XP_011529429.1:p.Ile1977Val
XM_011531128.1:c.5905A>G	XP_011529430.1:p.Ile1969Val
XM_011531129.1:c.5851A>G	XP_011529431.1:p.Ile1951Val
XM_011531130.1:c.5827A>G	XP_011529432.1:p.Ile1943Val
XM_011531131.1:c.5824A>G	XP_011529433.1:p.Ile1942Val
NM_001110556.2:c.6025A>G MANE Select	NP_001104026.1:p.Ile2009Val
NM_001456.4:c.6001A>G	NP_001447.2:p.Ile2001Val