Canonical Allele Identifier: CA519706137

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581282C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352914C>G , CM000685.2:g.154352914C>G	GRCh38
NC_000023.10:g.153581282C>G , CM000685.1:g.153581282C>G	GRCh37
NC_000023.9:g.153234476C>G	NCBI36
NG_011506.1:g.26725G>C
NG_011506.2:g.26725G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.6213G>C	ENSP00000353467.4:p.Gly2071=
ENST00000369850.10:c.6237G>C MANE Select	ENSP00000358866.3:p.Gly2079=
ENST00000369856.8:c.6156G>C	ENSP00000358872.4:p.Gly2052=
ENST00000422373.6:c.3161-239G>C	ENSP00000416926.2:n.3161-239G>C
ENST00000610817.5:c.6294G>C	ENSP00000480593.2:n.6294G>C
ENST00000673639.2:c.280-4224G>C
ENST00000676696.1:c.6516G>C	ENSP00000503392.1:n.6516G>C
ENST00000678304.1:n.1416G>C
ENST00000344736.8:c.6117G>C	ENSP00000358863.3:p.Gly2039=
ENST00000360319.8:c.6213G>C	ENSP00000353467.4:p.Gly2071=
ENST00000369850.7:c.6237G>C	ENSP00000358866.3:p.Gly2079=
ENST00000369856.7:c.6156G>C	ENSP00000358872.4:p.Gly2052=
ENST00000415241.1:c.439G>C
ENST00000420627.5:c.6193G>C	ENSP00000408921.1:n.6193G>C
ENST00000422373.5:c.6213G>C	ENSP00000416926.1:p.Gly2071=
ENST00000444578.1:c.180G>C	ENSP00000397824.1:p.Gly60=
ENST00000466325.1:n.452G>C
ENST00000490936.5:n.2226G>C
ENST00000610817.4:c.5844+479G>C	ENSP00000480593.1:n.5844+479G>C
NM_001110556.1:c.6237G>C	NP_001104026.1:p.Gly2079=
NM_001456.3:c.6213G>C	NP_001447.2:p.Gly2071=
XM_011531127.1:c.6141G>C	XP_011529429.1:p.Gly2047=
XM_011531128.1:c.6117G>C	XP_011529430.1:p.Gly2039=
XM_011531129.1:c.6063G>C	XP_011529431.1:p.Gly2021=
XM_011531130.1:c.6039G>C	XP_011529432.1:p.Gly2013=
XM_011531131.1:c.6036G>C	XP_011529433.1:p.Gly2012=
NM_001110556.2:c.6237G>C MANE Select	NP_001104026.1:p.Gly2079=
NM_001456.4:c.6213G>C	NP_001447.2:p.Gly2071=