Canonical Allele Identifier: CA415192462

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581010C>A (hg19) ; chrX:g.154352642C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352642C>A , CM000685.2:g.154352642C>A	GRCh38
NC_000023.10:g.153581010C>A , CM000685.1:g.153581010C>A	GRCh37
NC_000023.9:g.153234204C>A	NCBI36
NG_011506.1:g.26997G>T
NG_011506.2:g.26997G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6389G>T	ENSP00000353467.4:p.Gly2130Val
ENST00000369850.10:c.6413G>T MANE Select	ENSP00000358866.3:p.Gly2138Val
ENST00000369856.8:c.6332G>T	ENSP00000358872.4:p.Gly2111Val
ENST00000422373.6:c.3194G>T	ENSP00000416926.2:p.Gly1065Val
ENST00000610817.5:c.6470G>T	ENSP00000480593.2:n.6470G>T
ENST00000673639.2:c.280-3952G>T
ENST00000676696.1:c.6692G>T	ENSP00000503392.1:n.6692G>T
ENST00000678304.1:n.1592G>T
ENST00000344736.8:c.6293G>T	ENSP00000358863.3:p.Gly2098Val
ENST00000360319.8:c.6389G>T	ENSP00000353467.4:p.Gly2130Val
ENST00000369850.7:c.6413G>T	ENSP00000358866.3:p.Gly2138Val
ENST00000369856.7:c.6332G>T	ENSP00000358872.4:p.Gly2111Val
ENST00000415241.1:c.615G>T
ENST00000420627.5:c.6369G>T	ENSP00000408921.1:n.6369G>T
ENST00000422373.5:c.6389G>T	ENSP00000416926.1:p.Gly2130Val
ENST00000444578.1:c.322+130G>T	ENSP00000397824.1:n.322+130G>T
ENST00000466325.1:n.724G>T
ENST00000474358.5:n.46G>T
ENST00000490936.5:n.2402G>T
ENST00000498411.1:n.67+175G>T
ENST00000610817.4:c.5845-692G>T	ENSP00000480593.1:n.5845-692G>T
NM_001110556.1:c.6413G>T	NP_001104026.1:p.Gly2138Val
NM_001456.3:c.6389G>T	NP_001447.2:p.Gly2130Val
XM_011531127.1:c.6317G>T	XP_011529429.1:p.Gly2106Val
XM_011531128.1:c.6293G>T	XP_011529430.1:p.Gly2098Val
XM_011531129.1:c.6239G>T	XP_011529431.1:p.Gly2080Val
XM_011531130.1:c.6215G>T	XP_011529432.1:p.Gly2072Val
XM_011531131.1:c.6212G>T	XP_011529433.1:p.Gly2071Val
NM_001110556.2:c.6413G>T MANE Select	NP_001104026.1:p.Gly2138Val
NM_001456.4:c.6389G>T	NP_001447.2:p.Gly2130Val