Canonical Allele Identifier: CA519706193

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581445A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353077A>C , CM000685.2:g.154353077A>C	GRCh38
NC_000023.10:g.153581445A>C , CM000685.1:g.153581445A>C	GRCh37
NC_000023.9:g.153234639A>C	NCBI36
NG_011506.1:g.26562T>G
NG_011506.2:g.26562T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6126T>G	ENSP00000353467.4:p.Val2042=
ENST00000369850.10:c.6150T>G MANE Select	ENSP00000358866.3:p.Val2050=
ENST00000369856.8:c.6069T>G	ENSP00000358872.4:p.Val2023=
ENST00000422373.6:c.3161-402T>G	ENSP00000416926.2:n.3161-402T>G
ENST00000610817.5:c.6207T>G	ENSP00000480593.2:n.6207T>G
ENST00000673639.2:c.280-4387T>G
ENST00000676696.1:c.6429T>G	ENSP00000503392.1:n.6429T>G
ENST00000678304.1:n.1329T>G
ENST00000344736.8:c.6030T>G	ENSP00000358863.3:p.Val2010=
ENST00000360319.8:c.6126T>G	ENSP00000353467.4:p.Val2042=
ENST00000369850.7:c.6150T>G	ENSP00000358866.3:p.Val2050=
ENST00000369856.7:c.6069T>G	ENSP00000358872.4:p.Val2023=
ENST00000415241.1:c.352T>G
ENST00000420627.5:c.6106T>G	ENSP00000408921.1:n.6106T>G
ENST00000422373.5:c.6126T>G	ENSP00000416926.1:p.Val2042=
ENST00000444578.1:c.93T>G	ENSP00000397824.1:p.Val31=
ENST00000466325.1:n.289T>G
ENST00000490936.5:n.2139T>G
ENST00000610817.4:c.5844+316T>G	ENSP00000480593.1:n.5844+316T>G
NM_001110556.1:c.6150T>G	NP_001104026.1:p.Val2050=
NM_001456.3:c.6126T>G	NP_001447.2:p.Val2042=
XM_011531127.1:c.6054T>G	XP_011529429.1:p.Val2018=
XM_011531128.1:c.6030T>G	XP_011529430.1:p.Val2010=
XM_011531129.1:c.5976T>G	XP_011529431.1:p.Val1992=
XM_011531130.1:c.5952T>G	XP_011529432.1:p.Val1984=
XM_011531131.1:c.5949T>G	XP_011529433.1:p.Val1983=
NM_001110556.2:c.6150T>G MANE Select	NP_001104026.1:p.Val2050=
NM_001456.4:c.6126T>G	NP_001447.2:p.Val2042=