Canonical Allele Identifier: CA519706936

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581716G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353348G>C , CM000685.2:g.154353348G>C	GRCh38
NC_000023.10:g.153581716G>C , CM000685.1:g.153581716G>C	GRCh37
NC_000023.9:g.153234910G>C	NCBI36
NG_011506.1:g.26291C>G
NG_011506.2:g.26291C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5946C>G	ENSP00000353467.4:p.Pro1982=
ENST00000369850.10:c.5970C>G MANE Select	ENSP00000358866.3:p.Pro1990=
ENST00000369856.8:c.5889C>G	ENSP00000358872.4:p.Pro1963=
ENST00000422373.6:c.3161-673C>G	ENSP00000416926.2:n.3161-673C>G
ENST00000610817.5:c.6027C>G	ENSP00000480593.2:n.6027C>G
ENST00000673639.2:c.280-4658C>G
ENST00000676696.1:c.6249C>G	ENSP00000503392.1:n.6249C>G
ENST00000678304.1:n.1149C>G
ENST00000344736.8:c.5850C>G	ENSP00000358863.3:p.Pro1950=
ENST00000360319.8:c.5946C>G	ENSP00000353467.4:p.Pro1982=
ENST00000369850.7:c.5970C>G	ENSP00000358866.3:p.Pro1990=
ENST00000369856.7:c.5889C>G	ENSP00000358872.4:p.Pro1963=
ENST00000415241.1:c.155C>G
ENST00000420627.5:c.5926C>G	ENSP00000408921.1:n.5926C>G
ENST00000422373.5:c.5946C>G	ENSP00000416926.1:p.Pro1982=
ENST00000438732.2:c.644C>G
ENST00000466325.1:n.109C>G
ENST00000490936.5:n.1959C>G
ENST00000610817.4:c.5844+45C>G	ENSP00000480593.1:n.5844+45C>G
NM_001110556.1:c.5970C>G	NP_001104026.1:p.Pro1990=
NM_001456.3:c.5946C>G	NP_001447.2:p.Pro1982=
XM_011531127.1:c.5874C>G	XP_011529429.1:p.Pro1958=
XM_011531128.1:c.5850C>G	XP_011529430.1:p.Pro1950=
XM_011531129.1:c.5796C>G	XP_011529431.1:p.Pro1932=
XM_011531130.1:c.5772C>G	XP_011529432.1:p.Pro1924=
XM_011531131.1:c.5769C>G	XP_011529433.1:p.Pro1923=
NM_001110556.2:c.5970C>G MANE Select	NP_001104026.1:p.Pro1990=
NM_001456.4:c.5946C>G	NP_001447.2:p.Pro1982=