Canonical Allele Identifier: CA10560114

Gene: FLNA

Linked Data

• dbSNP Id: rs782061936
• ExAC: X:153581188 G / A
• gnomAD v2: X-153581188-G-A
• gnomAD v4: X-154352820-G-A
• MyVariant Identifiers: chrX:g.153581188G>A (hg19) ; chrX:g.154352820G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352820G>A , CM000685.2:g.154352820G>A	GRCh38
NC_000023.10:g.153581188G>A , CM000685.1:g.153581188G>A	GRCh37
NC_000023.9:g.153234382G>A	NCBI36
NG_011506.1:g.26819C>T
NG_011506.2:g.26819C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.6307C>T	ENSP00000353467.4:p.Pro2103Ser
ENST00000369850.10:c.6331C>T MANE Select	ENSP00000358866.3:p.Pro2111Ser
ENST00000369856.8:c.6250C>T	ENSP00000358872.4:p.Pro2084Ser
ENST00000422373.6:c.3161-145C>T	ENSP00000416926.2:n.3161-145C>T
ENST00000610817.5:c.6388C>T	ENSP00000480593.2:n.6388C>T
ENST00000673639.2:c.280-4130C>T
ENST00000676696.1:c.6610C>T	ENSP00000503392.1:n.6610C>T
ENST00000678304.1:n.1510C>T
ENST00000344736.8:c.6211C>T	ENSP00000358863.3:p.Pro2071Ser
ENST00000360319.8:c.6307C>T	ENSP00000353467.4:p.Pro2103Ser
ENST00000369850.7:c.6331C>T	ENSP00000358866.3:p.Pro2111Ser
ENST00000369856.7:c.6250C>T	ENSP00000358872.4:p.Pro2084Ser
ENST00000415241.1:c.533C>T
ENST00000420627.5:c.6287C>T	ENSP00000408921.1:n.6287C>T
ENST00000422373.5:c.6307C>T	ENSP00000416926.1:p.Pro2103Ser
ENST00000444578.1:c.274C>T	ENSP00000397824.1:p.Pro92Ser
ENST00000466325.1:n.546C>T
ENST00000490936.5:n.2320C>T
ENST00000498411.1:n.64C>T
ENST00000610817.4:c.5844+573C>T	ENSP00000480593.1:n.5844+573C>T
NM_001110556.1:c.6331C>T	NP_001104026.1:p.Pro2111Ser
NM_001456.3:c.6307C>T	NP_001447.2:p.Pro2103Ser
XM_011531127.1:c.6235C>T	XP_011529429.1:p.Pro2079Ser
XM_011531128.1:c.6211C>T	XP_011529430.1:p.Pro2071Ser
XM_011531129.1:c.6157C>T	XP_011529431.1:p.Pro2053Ser
XM_011531130.1:c.6133C>T	XP_011529432.1:p.Pro2045Ser
XM_011531131.1:c.6130C>T	XP_011529433.1:p.Pro2044Ser
NM_001110556.2:c.6331C>T MANE Select	NP_001104026.1:p.Pro2111Ser
NM_001456.4:c.6307C>T	NP_001447.2:p.Pro2103Ser