Canonical Allele Identifier: CA221720

Gene: FLNA

Linked Data

• ClinVar Variation Id: 93762
• ClinVar RCV Id: RCV000176728 ; RCV003764758
• dbSNP Id: rs186214592
• COSMIC: COSM6243532 ; COSM6243533
• MyVariant Identifiers: chrX:g.153586868G>A (hg19) ; chrX:g.154358500G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154358500G>A , CM000685.2:g.154358500G>A	GRCh38
NC_000023.10:g.153586868G>A , CM000685.1:g.153586868G>A	GRCh37
NC_000023.9:g.153240062G>A	NCBI36
NG_011506.1:g.21139C>T
NG_011506.2:g.21139C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.4543C>T	ENSP00000353467.4:p.Arg1515Ter
ENST00000369850.10:c.4543C>T MANE Select	ENSP00000358866.3:p.Arg1515Ter
ENST00000369856.8:c.4462C>T	ENSP00000358872.4:p.Arg1488Ter
ENST00000422373.6:c.3160+2855C>T	ENSP00000416926.2:n.3160+2855C>T
ENST00000610817.5:c.4600C>T	ENSP00000480593.2:n.4600C>T
ENST00000673639.2:c.279+6936C>T
ENST00000676696.1:c.4822C>T	ENSP00000503392.1:n.4822C>T
ENST00000678304.1:n.148+589C>T
ENST00000344736.8:c.4543C>T	ENSP00000358863.3:p.Arg1515Ter
ENST00000360319.8:c.4543C>T	ENSP00000353467.4:p.Arg1515Ter
ENST00000369850.7:c.4543C>T	ENSP00000358866.3:p.Arg1515Ter
ENST00000369856.7:c.4462C>T	ENSP00000358872.4:p.Arg1488Ter
ENST00000420627.5:c.4499C>T	ENSP00000408921.1:n.4499C>T
ENST00000422373.5:c.4543C>T	ENSP00000416926.1:p.Arg1515Ter
ENST00000466319.1:n.165C>T
ENST00000490936.5:n.556C>T
ENST00000610817.4:c.4462C>T	ENSP00000480593.1:p.Arg1488Ter
NM_001110556.1:c.4543C>T	NP_001104026.1:p.Arg1515Ter
NM_001456.3:c.4543C>T	NP_001447.2:p.Arg1515Ter
XM_011531127.1:c.4543C>T	XP_011529429.1:p.Arg1515Ter
XM_011531128.1:c.4543C>T	XP_011529430.1:p.Arg1515Ter
XM_011531129.1:c.4543C>T	XP_011529431.1:p.Arg1515Ter
XM_011531130.1:c.4543C>T	XP_011529432.1:p.Arg1515Ter
XM_011531131.1:c.4342C>T	XP_011529433.1:p.Arg1448Ter
NM_001110556.2:c.4543C>T MANE Select	NP_001104026.1:p.Arg1515Ter
NM_001456.4:c.4543C>T	NP_001447.2:p.Arg1515Ter