Canonical Allele Identifier: CA519706534

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581003C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352635C>G , CM000685.2:g.154352635C>G	GRCh38
NC_000023.10:g.153581003C>G , CM000685.1:g.153581003C>G	GRCh37
NC_000023.9:g.153234197C>G	NCBI36
NG_011506.1:g.27004G>C
NG_011506.2:g.27004G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6396G>C	ENSP00000353467.4:p.Val2132=
ENST00000369850.10:c.6420G>C MANE Select	ENSP00000358866.3:p.Val2140=
ENST00000369856.8:c.6339G>C	ENSP00000358872.4:p.Val2113=
ENST00000422373.6:c.3201G>C	ENSP00000416926.2:p.Val1067=
ENST00000610817.5:c.6477G>C	ENSP00000480593.2:n.6477G>C
ENST00000673639.2:c.280-3945G>C
ENST00000676696.1:c.6699G>C	ENSP00000503392.1:n.6699G>C
ENST00000678304.1:n.1599G>C
ENST00000344736.8:c.6300G>C	ENSP00000358863.3:p.Val2100=
ENST00000360319.8:c.6396G>C	ENSP00000353467.4:p.Val2132=
ENST00000369850.7:c.6420G>C	ENSP00000358866.3:p.Val2140=
ENST00000369856.7:c.6339G>C	ENSP00000358872.4:p.Val2113=
ENST00000415241.1:c.622G>C
ENST00000420627.5:c.6376G>C	ENSP00000408921.1:n.6376G>C
ENST00000422373.5:c.6396G>C	ENSP00000416926.1:p.Val2132=
ENST00000444578.1:c.322+137G>C	ENSP00000397824.1:n.322+137G>C
ENST00000466325.1:n.731G>C
ENST00000474358.5:n.53G>C
ENST00000490936.5:n.2409G>C
ENST00000498411.1:n.67+182G>C
ENST00000610817.4:c.5845-685G>C	ENSP00000480593.1:n.5845-685G>C
NM_001110556.1:c.6420G>C	NP_001104026.1:p.Val2140=
NM_001456.3:c.6396G>C	NP_001447.2:p.Val2132=
XM_011531127.1:c.6324G>C	XP_011529429.1:p.Val2108=
XM_011531128.1:c.6300G>C	XP_011529430.1:p.Val2100=
XM_011531129.1:c.6246G>C	XP_011529431.1:p.Val2082=
XM_011531130.1:c.6222G>C	XP_011529432.1:p.Val2074=
XM_011531131.1:c.6219G>C	XP_011529433.1:p.Val2073=
NM_001110556.2:c.6420G>C MANE Select	NP_001104026.1:p.Val2140=
NM_001456.4:c.6396G>C	NP_001447.2:p.Val2132=