Canonical Allele Identifier: CA415196029

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581485A>C (hg19) ; chrX:g.154353117A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353117A>C , CM000685.2:g.154353117A>C	GRCh38
NC_000023.10:g.153581485A>C , CM000685.1:g.153581485A>C	GRCh37
NC_000023.9:g.153234679A>C	NCBI36
NG_011506.1:g.26522T>G
NG_011506.2:g.26522T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6086T>G	ENSP00000353467.4:p.Val2029Gly
ENST00000369850.10:c.6110T>G MANE Select	ENSP00000358866.3:p.Val2037Gly
ENST00000369856.8:c.6029T>G	ENSP00000358872.4:p.Val2010Gly
ENST00000422373.6:c.3161-442T>G	ENSP00000416926.2:n.3161-442T>G
ENST00000610817.5:c.6167T>G	ENSP00000480593.2:n.6167T>G
ENST00000673639.2:c.280-4427T>G
ENST00000676696.1:c.6389T>G	ENSP00000503392.1:n.6389T>G
ENST00000678304.1:n.1289T>G
ENST00000344736.8:c.5990T>G	ENSP00000358863.3:p.Val1997Gly
ENST00000360319.8:c.6086T>G	ENSP00000353467.4:p.Val2029Gly
ENST00000369850.7:c.6110T>G	ENSP00000358866.3:p.Val2037Gly
ENST00000369856.7:c.6029T>G	ENSP00000358872.4:p.Val2010Gly
ENST00000415241.1:c.312T>G
ENST00000420627.5:c.6066T>G	ENSP00000408921.1:n.6066T>G
ENST00000422373.5:c.6086T>G	ENSP00000416926.1:p.Val2029Gly
ENST00000444578.1:c.53T>G	ENSP00000397824.1:p.Val18Gly
ENST00000466325.1:n.249T>G
ENST00000490936.5:n.2099T>G
ENST00000610817.4:c.5844+276T>G	ENSP00000480593.1:n.5844+276T>G
NM_001110556.1:c.6110T>G	NP_001104026.1:p.Val2037Gly
NM_001456.3:c.6086T>G	NP_001447.2:p.Val2029Gly
XM_011531127.1:c.6014T>G	XP_011529429.1:p.Val2005Gly
XM_011531128.1:c.5990T>G	XP_011529430.1:p.Val1997Gly
XM_011531129.1:c.5936T>G	XP_011529431.1:p.Val1979Gly
XM_011531130.1:c.5912T>G	XP_011529432.1:p.Val1971Gly
XM_011531131.1:c.5909T>G	XP_011529433.1:p.Val1970Gly
NM_001110556.2:c.6110T>G MANE Select	NP_001104026.1:p.Val2037Gly
NM_001456.4:c.6086T>G	NP_001447.2:p.Val2029Gly