Canonical Allele Identifier: CA415197338

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581711C>T (hg19) ; chrX:g.154353343C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353343C>T , CM000685.2:g.154353343C>T	GRCh38
NC_000023.10:g.153581711C>T , CM000685.1:g.153581711C>T	GRCh37
NC_000023.9:g.153234905C>T	NCBI36
NG_011506.1:g.26296G>A
NG_011506.2:g.26296G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5951G>A	ENSP00000353467.4:p.Gly1984Asp
ENST00000369850.10:c.5975G>A MANE Select	ENSP00000358866.3:p.Gly1992Asp
ENST00000369856.8:c.5894G>A	ENSP00000358872.4:p.Gly1965Asp
ENST00000422373.6:c.3161-668G>A	ENSP00000416926.2:n.3161-668G>A
ENST00000610817.5:c.6032G>A	ENSP00000480593.2:n.6032G>A
ENST00000673639.2:c.280-4653G>A
ENST00000676696.1:c.6254G>A	ENSP00000503392.1:n.6254G>A
ENST00000678304.1:n.1154G>A
ENST00000344736.8:c.5855G>A	ENSP00000358863.3:p.Gly1952Asp
ENST00000360319.8:c.5951G>A	ENSP00000353467.4:p.Gly1984Asp
ENST00000369850.7:c.5975G>A	ENSP00000358866.3:p.Gly1992Asp
ENST00000369856.7:c.5894G>A	ENSP00000358872.4:p.Gly1965Asp
ENST00000415241.1:c.160G>A
ENST00000420627.5:c.5931G>A	ENSP00000408921.1:n.5931G>A
ENST00000422373.5:c.5951G>A	ENSP00000416926.1:p.Gly1984Asp
ENST00000438732.2:c.649G>A
ENST00000466325.1:n.114G>A
ENST00000490936.5:n.1964G>A
ENST00000610817.4:c.5844+50G>A	ENSP00000480593.1:n.5844+50G>A
NM_001110556.1:c.5975G>A	NP_001104026.1:p.Gly1992Asp
NM_001456.3:c.5951G>A	NP_001447.2:p.Gly1984Asp
XM_011531127.1:c.5879G>A	XP_011529429.1:p.Gly1960Asp
XM_011531128.1:c.5855G>A	XP_011529430.1:p.Gly1952Asp
XM_011531129.1:c.5801G>A	XP_011529431.1:p.Gly1934Asp
XM_011531130.1:c.5777G>A	XP_011529432.1:p.Gly1926Asp
XM_011531131.1:c.5774G>A	XP_011529433.1:p.Gly1925Asp
NM_001110556.2:c.5975G>A MANE Select	NP_001104026.1:p.Gly1992Asp
NM_001456.4:c.5951G>A	NP_001447.2:p.Gly1984Asp