Canonical Allele Identifier: CA415197254

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581701C>A (hg19) ; chrX:g.154353333C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353333C>A , CM000685.2:g.154353333C>A	GRCh38
NC_000023.10:g.153581701C>A , CM000685.1:g.153581701C>A	GRCh37
NC_000023.9:g.153234895C>A	NCBI36
NG_011506.1:g.26306G>T
NG_011506.2:g.26306G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5961G>T	ENSP00000353467.4:p.Glu1987Asp
ENST00000369850.10:c.5985G>T MANE Select	ENSP00000358866.3:p.Glu1995Asp
ENST00000369856.8:c.5904G>T	ENSP00000358872.4:p.Glu1968Asp
ENST00000422373.6:c.3161-658G>T	ENSP00000416926.2:n.3161-658G>T
ENST00000610817.5:c.6042G>T	ENSP00000480593.2:n.6042G>T
ENST00000673639.2:c.280-4643G>T
ENST00000676696.1:c.6264G>T	ENSP00000503392.1:n.6264G>T
ENST00000678304.1:n.1164G>T
ENST00000344736.8:c.5865G>T	ENSP00000358863.3:p.Glu1955Asp
ENST00000360319.8:c.5961G>T	ENSP00000353467.4:p.Glu1987Asp
ENST00000369850.7:c.5985G>T	ENSP00000358866.3:p.Glu1995Asp
ENST00000369856.7:c.5904G>T	ENSP00000358872.4:p.Glu1968Asp
ENST00000415241.1:c.170G>T
ENST00000420627.5:c.5941G>T	ENSP00000408921.1:n.5941G>T
ENST00000422373.5:c.5961G>T	ENSP00000416926.1:p.Glu1987Asp
ENST00000438732.2:c.659G>T
ENST00000466325.1:n.124G>T
ENST00000490936.5:n.1974G>T
ENST00000610817.4:c.5844+60G>T	ENSP00000480593.1:n.5844+60G>T
NM_001110556.1:c.5985G>T	NP_001104026.1:p.Glu1995Asp
NM_001456.3:c.5961G>T	NP_001447.2:p.Glu1987Asp
XM_011531127.1:c.5889G>T	XP_011529429.1:p.Glu1963Asp
XM_011531128.1:c.5865G>T	XP_011529430.1:p.Glu1955Asp
XM_011531129.1:c.5811G>T	XP_011529431.1:p.Glu1937Asp
XM_011531130.1:c.5787G>T	XP_011529432.1:p.Glu1929Asp
XM_011531131.1:c.5784G>T	XP_011529433.1:p.Glu1928Asp
NM_001110556.2:c.5985G>T MANE Select	NP_001104026.1:p.Glu1995Asp
NM_001456.4:c.5961G>T	NP_001447.2:p.Glu1987Asp