Canonical Allele Identifier: CA415194911

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581369C>G (hg19) ; chrX:g.154353001C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353001C>G , CM000685.2:g.154353001C>G	GRCh38
NC_000023.10:g.153581369C>G , CM000685.1:g.153581369C>G	GRCh37
NC_000023.9:g.153234563C>G	NCBI36
NG_011506.1:g.26638G>C
NG_011506.2:g.26638G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6202G>C	ENSP00000353467.4:p.Gly2068Arg
ENST00000369850.10:c.6226G>C MANE Select	ENSP00000358866.3:p.Gly2076Arg
ENST00000369856.8:c.6145G>C	ENSP00000358872.4:p.Gly2049Arg
ENST00000422373.6:c.3161-326G>C	ENSP00000416926.2:n.3161-326G>C
ENST00000610817.5:c.6283G>C	ENSP00000480593.2:n.6283G>C
ENST00000673639.2:c.280-4311G>C
ENST00000676696.1:c.6505G>C	ENSP00000503392.1:n.6505G>C
ENST00000678304.1:n.1405G>C
ENST00000344736.8:c.6106G>C	ENSP00000358863.3:p.Gly2036Arg
ENST00000360319.8:c.6202G>C	ENSP00000353467.4:p.Gly2068Arg
ENST00000369850.7:c.6226G>C	ENSP00000358866.3:p.Gly2076Arg
ENST00000369856.7:c.6145G>C	ENSP00000358872.4:p.Gly2049Arg
ENST00000415241.1:c.428G>C
ENST00000420627.5:c.6182G>C	ENSP00000408921.1:n.6182G>C
ENST00000422373.5:c.6202G>C	ENSP00000416926.1:p.Gly2068Arg
ENST00000444578.1:c.169G>C	ENSP00000397824.1:p.Gly57Arg
ENST00000466325.1:n.365G>C
ENST00000490936.5:n.2215G>C
ENST00000610817.4:c.5844+392G>C	ENSP00000480593.1:n.5844+392G>C
NM_001110556.1:c.6226G>C	NP_001104026.1:p.Gly2076Arg
NM_001456.3:c.6202G>C	NP_001447.2:p.Gly2068Arg
XM_011531127.1:c.6130G>C	XP_011529429.1:p.Gly2044Arg
XM_011531128.1:c.6106G>C	XP_011529430.1:p.Gly2036Arg
XM_011531129.1:c.6052G>C	XP_011529431.1:p.Gly2018Arg
XM_011531130.1:c.6028G>C	XP_011529432.1:p.Gly2010Arg
XM_011531131.1:c.6025G>C	XP_011529433.1:p.Gly2009Arg
NM_001110556.2:c.6226G>C MANE Select	NP_001104026.1:p.Gly2076Arg
NM_001456.4:c.6202G>C	NP_001447.2:p.Gly2068Arg