Canonical Allele Identifier: CA10560264

Gene: FLNA

Linked Data

• ClinVar Variation Id: 515378
• ClinVar RCV Id: RCV000603707 ; RCV003767707
• dbSNP Id: rs782669152
• ExAC: X:153582307 C / T
• gnomAD v2: X-153582307-C-T
• gnomAD v4: X-154353939-C-T
• MyVariant Identifiers: chrX:g.153582307C>T (hg19) ; chrX:g.154353939C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353939C>T , CM000685.2:g.154353939C>T	GRCh38
NC_000023.10:g.153582307C>T , CM000685.1:g.153582307C>T	GRCh37
NC_000023.9:g.153235501C>T	NCBI36
NG_011506.1:g.25700G>A
NG_011506.2:g.25700G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5638G>A	ENSP00000353467.4:p.Val1880Ile
ENST00000369850.10:c.5662G>A MANE Select	ENSP00000358866.3:p.Val1888Ile
ENST00000369856.8:c.5581G>A	ENSP00000358872.4:p.Val1861Ile
ENST00000422373.6:c.3161-1264G>A	ENSP00000416926.2:n.3161-1264G>A
ENST00000610817.5:c.5719G>A	ENSP00000480593.2:n.5719G>A
ENST00000673639.2:c.280-5249G>A
ENST00000676696.1:c.5941G>A	ENSP00000503392.1:n.5941G>A
ENST00000678304.1:n.841G>A
ENST00000344736.8:c.5542G>A	ENSP00000358863.3:p.Val1848Ile
ENST00000360319.8:c.5638G>A	ENSP00000353467.4:p.Val1880Ile
ENST00000369850.7:c.5662G>A	ENSP00000358866.3:p.Val1888Ile
ENST00000369856.7:c.5581G>A	ENSP00000358872.4:p.Val1861Ile
ENST00000420627.5:c.5618G>A	ENSP00000408921.1:n.5618G>A
ENST00000422373.5:c.5638G>A	ENSP00000416926.1:p.Val1880Ile
ENST00000438732.2:c.510G>A
ENST00000490936.5:n.1651G>A
ENST00000610817.4:c.5581G>A	ENSP00000480593.1:p.Val1861Ile
NM_001110556.1:c.5662G>A	NP_001104026.1:p.Val1888Ile
NM_001456.3:c.5638G>A	NP_001447.2:p.Val1880Ile
XM_011531127.1:c.5566G>A	XP_011529429.1:p.Val1856Ile
XM_011531128.1:c.5542G>A	XP_011529430.1:p.Val1848Ile
XM_011531129.1:c.5662G>A	XP_011529431.1:p.Val1888Ile
XM_011531130.1:c.5638G>A	XP_011529432.1:p.Val1880Ile
XM_011531131.1:c.5461G>A	XP_011529433.1:p.Val1821Ile
NM_001110556.2:c.5662G>A MANE Select	NP_001104026.1:p.Val1888Ile
NM_001456.4:c.5638G>A	NP_001447.2:p.Val1880Ile