Canonical Allele Identifier: CA415194662

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581284C>T (hg19) ; chrX:g.154352916C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352916C>T , CM000685.2:g.154352916C>T	GRCh38
NC_000023.10:g.153581284C>T , CM000685.1:g.153581284C>T	GRCh37
NC_000023.9:g.153234478C>T	NCBI36
NG_011506.1:g.26723G>A
NG_011506.2:g.26723G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.6211G>A	ENSP00000353467.4:p.Gly2071Arg
ENST00000369850.10:c.6235G>A MANE Select	ENSP00000358866.3:p.Gly2079Arg
ENST00000369856.8:c.6154G>A	ENSP00000358872.4:p.Gly2052Arg
ENST00000422373.6:c.3161-241G>A	ENSP00000416926.2:n.3161-241G>A
ENST00000610817.5:c.6292G>A	ENSP00000480593.2:n.6292G>A
ENST00000673639.2:c.280-4226G>A
ENST00000676696.1:c.6514G>A	ENSP00000503392.1:n.6514G>A
ENST00000678304.1:n.1414G>A
ENST00000344736.8:c.6115G>A	ENSP00000358863.3:p.Gly2039Arg
ENST00000360319.8:c.6211G>A	ENSP00000353467.4:p.Gly2071Arg
ENST00000369850.7:c.6235G>A	ENSP00000358866.3:p.Gly2079Arg
ENST00000369856.7:c.6154G>A	ENSP00000358872.4:p.Gly2052Arg
ENST00000415241.1:c.437G>A
ENST00000420627.5:c.6191G>A	ENSP00000408921.1:n.6191G>A
ENST00000422373.5:c.6211G>A	ENSP00000416926.1:p.Gly2071Arg
ENST00000444578.1:c.178G>A	ENSP00000397824.1:p.Gly60Arg
ENST00000466325.1:n.450G>A
ENST00000490936.5:n.2224G>A
ENST00000610817.4:c.5844+477G>A	ENSP00000480593.1:n.5844+477G>A
NM_001110556.1:c.6235G>A	NP_001104026.1:p.Gly2079Arg
NM_001456.3:c.6211G>A	NP_001447.2:p.Gly2071Arg
XM_011531127.1:c.6139G>A	XP_011529429.1:p.Gly2047Arg
XM_011531128.1:c.6115G>A	XP_011529430.1:p.Gly2039Arg
XM_011531129.1:c.6061G>A	XP_011529431.1:p.Gly2021Arg
XM_011531130.1:c.6037G>A	XP_011529432.1:p.Gly2013Arg
XM_011531131.1:c.6034G>A	XP_011529433.1:p.Gly2012Arg
NM_001110556.2:c.6235G>A MANE Select	NP_001104026.1:p.Gly2079Arg
NM_001456.4:c.6211G>A	NP_001447.2:p.Gly2071Arg