Canonical Allele Identifier: CA415193920

Gene: FLNA

Linked Data

• gnomAD v4: X-154352855-T-C
• MyVariant Identifiers: chrX:g.153581223T>C (hg19) ; chrX:g.154352855T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352855T>C , CM000685.2:g.154352855T>C	GRCh38
NC_000023.10:g.153581223T>C , CM000685.1:g.153581223T>C	GRCh37
NC_000023.9:g.153234417T>C	NCBI36
NG_011506.1:g.26784A>G
NG_011506.2:g.26784A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6272A>G	ENSP00000353467.4:p.Asp2091Gly
ENST00000369850.10:c.6296A>G MANE Select	ENSP00000358866.3:p.Asp2099Gly
ENST00000369856.8:c.6215A>G	ENSP00000358872.4:p.Asp2072Gly
ENST00000422373.6:c.3161-180A>G	ENSP00000416926.2:n.3161-180A>G
ENST00000610817.5:c.6353A>G	ENSP00000480593.2:n.6353A>G
ENST00000673639.2:c.280-4165A>G
ENST00000676696.1:c.6575A>G	ENSP00000503392.1:n.6575A>G
ENST00000678304.1:n.1475A>G
ENST00000344736.8:c.6176A>G	ENSP00000358863.3:p.Asp2059Gly
ENST00000360319.8:c.6272A>G	ENSP00000353467.4:p.Asp2091Gly
ENST00000369850.7:c.6296A>G	ENSP00000358866.3:p.Asp2099Gly
ENST00000369856.7:c.6215A>G	ENSP00000358872.4:p.Asp2072Gly
ENST00000415241.1:c.498A>G
ENST00000420627.5:c.6252A>G	ENSP00000408921.1:n.6252A>G
ENST00000422373.5:c.6272A>G	ENSP00000416926.1:p.Asp2091Gly
ENST00000444578.1:c.239A>G	ENSP00000397824.1:p.Asp80Gly
ENST00000466325.1:n.511A>G
ENST00000490936.5:n.2285A>G
ENST00000498411.1:n.29A>G
ENST00000610817.4:c.5844+538A>G	ENSP00000480593.1:n.5844+538A>G
NM_001110556.1:c.6296A>G	NP_001104026.1:p.Asp2099Gly
NM_001456.3:c.6272A>G	NP_001447.2:p.Asp2091Gly
XM_011531127.1:c.6200A>G	XP_011529429.1:p.Asp2067Gly
XM_011531128.1:c.6176A>G	XP_011529430.1:p.Asp2059Gly
XM_011531129.1:c.6122A>G	XP_011529431.1:p.Asp2041Gly
XM_011531130.1:c.6098A>G	XP_011529432.1:p.Asp2033Gly
XM_011531131.1:c.6095A>G	XP_011529433.1:p.Asp2032Gly
NM_001110556.2:c.6296A>G MANE Select	NP_001104026.1:p.Asp2099Gly
NM_001456.4:c.6272A>G	NP_001447.2:p.Asp2091Gly