Canonical Allele Identifier: CA415195713

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581441C>A (hg19) ; chrX:g.154353073C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353073C>A , CM000685.2:g.154353073C>A	GRCh38
NC_000023.10:g.153581441C>A , CM000685.1:g.153581441C>A	GRCh37
NC_000023.9:g.153234635C>A	NCBI36
NG_011506.1:g.26566G>T
NG_011506.2:g.26566G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6130G>T	ENSP00000353467.4:p.Val2044Phe
ENST00000369850.10:c.6154G>T MANE Select	ENSP00000358866.3:p.Val2052Phe
ENST00000369856.8:c.6073G>T	ENSP00000358872.4:p.Val2025Phe
ENST00000422373.6:c.3161-398G>T	ENSP00000416926.2:n.3161-398G>T
ENST00000610817.5:c.6211G>T	ENSP00000480593.2:n.6211G>T
ENST00000673639.2:c.280-4383G>T
ENST00000676696.1:c.6433G>T	ENSP00000503392.1:n.6433G>T
ENST00000678304.1:n.1333G>T
ENST00000344736.8:c.6034G>T	ENSP00000358863.3:p.Val2012Phe
ENST00000360319.8:c.6130G>T	ENSP00000353467.4:p.Val2044Phe
ENST00000369850.7:c.6154G>T	ENSP00000358866.3:p.Val2052Phe
ENST00000369856.7:c.6073G>T	ENSP00000358872.4:p.Val2025Phe
ENST00000415241.1:c.356G>T
ENST00000420627.5:c.6110G>T	ENSP00000408921.1:n.6110G>T
ENST00000422373.5:c.6130G>T	ENSP00000416926.1:p.Val2044Phe
ENST00000444578.1:c.97G>T	ENSP00000397824.1:p.Val33Phe
ENST00000466325.1:n.293G>T
ENST00000490936.5:n.2143G>T
ENST00000610817.4:c.5844+320G>T	ENSP00000480593.1:n.5844+320G>T
NM_001110556.1:c.6154G>T	NP_001104026.1:p.Val2052Phe
NM_001456.3:c.6130G>T	NP_001447.2:p.Val2044Phe
XM_011531127.1:c.6058G>T	XP_011529429.1:p.Val2020Phe
XM_011531128.1:c.6034G>T	XP_011529430.1:p.Val2012Phe
XM_011531129.1:c.5980G>T	XP_011529431.1:p.Val1994Phe
XM_011531130.1:c.5956G>T	XP_011529432.1:p.Val1986Phe
XM_011531131.1:c.5953G>T	XP_011529433.1:p.Val1985Phe
NM_001110556.2:c.6154G>T MANE Select	NP_001104026.1:p.Val2052Phe
NM_001456.4:c.6130G>T	NP_001447.2:p.Val2044Phe