Canonical Allele Identifier: CA519706556

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581021C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352653C>G , CM000685.2:g.154352653C>G	GRCh38
NC_000023.10:g.153581021C>G , CM000685.1:g.153581021C>G	GRCh37
NC_000023.9:g.153234215C>G	NCBI36
NG_011506.1:g.26986G>C
NG_011506.2:g.26986G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6378G>C	ENSP00000353467.4:p.Val2126=
ENST00000369850.10:c.6402G>C MANE Select	ENSP00000358866.3:p.Val2134=
ENST00000369856.8:c.6321G>C	ENSP00000358872.4:p.Val2107=
ENST00000422373.6:c.3183G>C	ENSP00000416926.2:p.Val1061=
ENST00000610817.5:c.6459G>C	ENSP00000480593.2:n.6459G>C
ENST00000673639.2:c.280-3963G>C
ENST00000676696.1:c.6681G>C	ENSP00000503392.1:n.6681G>C
ENST00000678304.1:n.1581G>C
ENST00000344736.8:c.6282G>C	ENSP00000358863.3:p.Val2094=
ENST00000360319.8:c.6378G>C	ENSP00000353467.4:p.Val2126=
ENST00000369850.7:c.6402G>C	ENSP00000358866.3:p.Val2134=
ENST00000369856.7:c.6321G>C	ENSP00000358872.4:p.Val2107=
ENST00000415241.1:c.604G>C
ENST00000420627.5:c.6358G>C	ENSP00000408921.1:n.6358G>C
ENST00000422373.5:c.6378G>C	ENSP00000416926.1:p.Val2126=
ENST00000444578.1:c.322+119G>C	ENSP00000397824.1:n.322+119G>C
ENST00000466325.1:n.713G>C
ENST00000474358.5:n.35G>C
ENST00000490936.5:n.2391G>C
ENST00000498411.1:n.67+164G>C
ENST00000610817.4:c.5845-703G>C	ENSP00000480593.1:n.5845-703G>C
NM_001110556.1:c.6402G>C	NP_001104026.1:p.Val2134=
NM_001456.3:c.6378G>C	NP_001447.2:p.Val2126=
XM_011531127.1:c.6306G>C	XP_011529429.1:p.Val2102=
XM_011531128.1:c.6282G>C	XP_011529430.1:p.Val2094=
XM_011531129.1:c.6228G>C	XP_011529431.1:p.Val2076=
XM_011531130.1:c.6204G>C	XP_011529432.1:p.Val2068=
XM_011531131.1:c.6201G>C	XP_011529433.1:p.Val2067=
NM_001110556.2:c.6402G>C MANE Select	NP_001104026.1:p.Val2134=
NM_001456.4:c.6378G>C	NP_001447.2:p.Val2126=