Canonical Allele Identifier: CA519706099

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581216C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352848C>G , CM000685.2:g.154352848C>G	GRCh38
NC_000023.10:g.153581216C>G , CM000685.1:g.153581216C>G	GRCh37
NC_000023.9:g.153234410C>G	NCBI36
NG_011506.1:g.26791G>C
NG_011506.2:g.26791G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6279G>C	ENSP00000353467.4:p.Thr2093=
ENST00000369850.10:c.6303G>C MANE Select	ENSP00000358866.3:p.Thr2101=
ENST00000369856.8:c.6222G>C	ENSP00000358872.4:p.Thr2074=
ENST00000422373.6:c.3161-173G>C	ENSP00000416926.2:n.3161-173G>C
ENST00000610817.5:c.6360G>C	ENSP00000480593.2:n.6360G>C
ENST00000673639.2:c.280-4158G>C
ENST00000676696.1:c.6582G>C	ENSP00000503392.1:n.6582G>C
ENST00000678304.1:n.1482G>C
ENST00000344736.8:c.6183G>C	ENSP00000358863.3:p.Thr2061=
ENST00000360319.8:c.6279G>C	ENSP00000353467.4:p.Thr2093=
ENST00000369850.7:c.6303G>C	ENSP00000358866.3:p.Thr2101=
ENST00000369856.7:c.6222G>C	ENSP00000358872.4:p.Thr2074=
ENST00000415241.1:c.505G>C
ENST00000420627.5:c.6259G>C	ENSP00000408921.1:n.6259G>C
ENST00000422373.5:c.6279G>C	ENSP00000416926.1:p.Thr2093=
ENST00000444578.1:c.246G>C	ENSP00000397824.1:p.Thr82=
ENST00000466325.1:n.518G>C
ENST00000490936.5:n.2292G>C
ENST00000498411.1:n.36G>C
ENST00000610817.4:c.5844+545G>C	ENSP00000480593.1:n.5844+545G>C
NM_001110556.1:c.6303G>C	NP_001104026.1:p.Thr2101=
NM_001456.3:c.6279G>C	NP_001447.2:p.Thr2093=
XM_011531127.1:c.6207G>C	XP_011529429.1:p.Thr2069=
XM_011531128.1:c.6183G>C	XP_011529430.1:p.Thr2061=
XM_011531129.1:c.6129G>C	XP_011529431.1:p.Thr2043=
XM_011531130.1:c.6105G>C	XP_011529432.1:p.Thr2035=
XM_011531131.1:c.6102G>C	XP_011529433.1:p.Thr2034=
NM_001110556.2:c.6303G>C MANE Select	NP_001104026.1:p.Thr2101=
NM_001456.4:c.6279G>C	NP_001447.2:p.Thr2093=