Canonical Allele Identifier: CA519706733

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581544C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353176C>G , CM000685.2:g.154353176C>G	GRCh38
NC_000023.10:g.153581544C>G , CM000685.1:g.153581544C>G	GRCh37
NC_000023.9:g.153234738C>G	NCBI36
NG_011506.1:g.26463G>C
NG_011506.2:g.26463G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6027G>C	ENSP00000353467.4:p.Gly2009=
ENST00000369850.10:c.6051G>C MANE Select	ENSP00000358866.3:p.Gly2017=
ENST00000369856.8:c.5970G>C	ENSP00000358872.4:p.Gly1990=
ENST00000422373.6:c.3161-501G>C	ENSP00000416926.2:n.3161-501G>C
ENST00000610817.5:c.6108G>C	ENSP00000480593.2:n.6108G>C
ENST00000673639.2:c.280-4486G>C
ENST00000676696.1:c.6330G>C	ENSP00000503392.1:n.6330G>C
ENST00000678304.1:n.1230G>C
ENST00000344736.8:c.5931G>C	ENSP00000358863.3:p.Gly1977=
ENST00000360319.8:c.6027G>C	ENSP00000353467.4:p.Gly2009=
ENST00000369850.7:c.6051G>C	ENSP00000358866.3:p.Gly2017=
ENST00000369856.7:c.5970G>C	ENSP00000358872.4:p.Gly1990=
ENST00000415241.1:c.253G>C
ENST00000420627.5:c.6007G>C	ENSP00000408921.1:n.6007G>C
ENST00000422373.5:c.6027G>C	ENSP00000416926.1:p.Gly2009=
ENST00000466325.1:n.190G>C
ENST00000490936.5:n.2040G>C
ENST00000610817.4:c.5844+217G>C	ENSP00000480593.1:n.5844+217G>C
NM_001110556.1:c.6051G>C	NP_001104026.1:p.Gly2017=
NM_001456.3:c.6027G>C	NP_001447.2:p.Gly2009=
XM_011531127.1:c.5955G>C	XP_011529429.1:p.Gly1985=
XM_011531128.1:c.5931G>C	XP_011529430.1:p.Gly1977=
XM_011531129.1:c.5877G>C	XP_011529431.1:p.Gly1959=
XM_011531130.1:c.5853G>C	XP_011529432.1:p.Gly1951=
XM_011531131.1:c.5850G>C	XP_011529433.1:p.Gly1950=
NM_001110556.2:c.6051G>C MANE Select	NP_001104026.1:p.Gly2017=
NM_001456.4:c.6027G>C	NP_001447.2:p.Gly2009=