Canonical Allele Identifier: CA10560184

Gene: FLNA

Linked Data

• dbSNP Id: rs782264106
• ExAC: X:153581652 T / TCAGCCGCTTACCCACGTGGCCATTACG
• gnomAD v4: X-154353284-T-TCAGCCGCTTACCCACGTGGCCATTACG
• MyVariant Identifiers: chrX:g.153581652_153581653insCAGCCGCTTACCCACGTGGCCATTACG (hg19) ; chrX:g.154353284_154353285insCAGCCGCTTACCCACGTGGCCATTACG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353294_154353320dup , CM000685.2:g.154353294_154353320dup	GRCh38
NC_000023.10:g.153581662_153581688dup , CM000685.1:g.153581662_153581688dup	GRCh37
NC_000023.9:g.153234856_153234882dup	NCBI36
NG_011506.1:g.26328_26354dup
NG_011506.2:g.26328_26354dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5983_5998+11dup
ENST00000369850.10:c.6007_6022+11dup
ENST00000369856.8:c.5926_5941+11dup
ENST00000422373.6:c.3161-636_3161-610dup	ENSP00000416926.2:n.3161-636_3161-610dup
ENST00000610817.5:c.6064_6079+11dup
ENST00000673639.2:c.280-4621_280-4595dup
ENST00000676696.1:c.6286_6301+11dup
ENST00000678304.1:n.1186_1201+11dup
ENST00000344736.8:c.5887_5902+11dup
ENST00000360319.8:c.5983_5998+11dup
ENST00000369850.7:c.6007_6022+11dup
ENST00000369856.7:c.5926_5941+11dup
ENST00000415241.1:c.192_207+11dup
ENST00000420627.5:c.5963_5978+11dup
ENST00000422373.5:c.5983_5998+11dup
ENST00000466325.1:n.146_161+11dup
ENST00000490936.5:n.1996_2011+11dup
ENST00000610817.4:c.5844+82_5844+108dup	ENSP00000480593.1:n.5844+82_5844+108dup
NM_001110556.1:c.6007_6022+11dup
NM_001456.3:c.5983_5998+11dup
XM_011531127.1:c.5911_5926+11dup
XM_011531128.1:c.5887_5902+11dup
XM_011531129.1:c.5833_5848+11dup
XM_011531130.1:c.5809_5824+11dup
XM_011531131.1:c.5806_5821+11dup
NM_001110556.2:c.6007_6022+11dup
NM_001456.4:c.5983_5998+11dup