Canonical Allele Identifier: CA519706837

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581671G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353303G>C , CM000685.2:g.154353303G>C	GRCh38
NC_000023.10:g.153581671G>C , CM000685.1:g.153581671G>C	GRCh37
NC_000023.9:g.153234865G>C	NCBI36
NG_011506.1:g.26336C>G
NG_011506.2:g.26336C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5991C>G	ENSP00000353467.4:p.Gly1997=
ENST00000369850.10:c.6015C>G MANE Select	ENSP00000358866.3:p.Gly2005=
ENST00000369856.8:c.5934C>G	ENSP00000358872.4:p.Gly1978=
ENST00000422373.6:c.3161-628C>G	ENSP00000416926.2:n.3161-628C>G
ENST00000610817.5:c.6072C>G	ENSP00000480593.2:n.6072C>G
ENST00000673639.2:c.280-4613C>G
ENST00000676696.1:c.6294C>G	ENSP00000503392.1:n.6294C>G
ENST00000678304.1:n.1194C>G
ENST00000344736.8:c.5895C>G	ENSP00000358863.3:p.Gly1965=
ENST00000360319.8:c.5991C>G	ENSP00000353467.4:p.Gly1997=
ENST00000369850.7:c.6015C>G	ENSP00000358866.3:p.Gly2005=
ENST00000369856.7:c.5934C>G	ENSP00000358872.4:p.Gly1978=
ENST00000415241.1:c.200C>G
ENST00000420627.5:c.5971C>G	ENSP00000408921.1:n.5971C>G
ENST00000422373.5:c.5991C>G	ENSP00000416926.1:p.Gly1997=
ENST00000438732.2:c.689C>G
ENST00000466325.1:n.154C>G
ENST00000490936.5:n.2004C>G
ENST00000610817.4:c.5844+90C>G	ENSP00000480593.1:n.5844+90C>G
NM_001110556.1:c.6015C>G	NP_001104026.1:p.Gly2005=
NM_001456.3:c.5991C>G	NP_001447.2:p.Gly1997=
XM_011531127.1:c.5919C>G	XP_011529429.1:p.Gly1973=
XM_011531128.1:c.5895C>G	XP_011529430.1:p.Gly1965=
XM_011531129.1:c.5841C>G	XP_011529431.1:p.Gly1947=
XM_011531130.1:c.5817C>G	XP_011529432.1:p.Gly1939=
XM_011531131.1:c.5814C>G	XP_011529433.1:p.Gly1938=
NM_001110556.2:c.6015C>G MANE Select	NP_001104026.1:p.Gly2005=
NM_001456.4:c.5991C>G	NP_001447.2:p.Gly1997=