Canonical Allele Identifier: CA519707740

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153586724_153586812del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154358358_154358446del , CM000685.2:g.154358358_154358446del	GRCh38
NC_000023.10:g.153586726_153586814del , CM000685.1:g.153586726_153586814del	GRCh37
NC_000023.9:g.153239920_153240008del	NCBI36
NG_011506.1:g.21195_21283del
NG_011506.2:g.21195_21283del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.4598+1_4599-1del
ENST00000369850.10:c.4598+1_4599-1del
ENST00000369856.8:c.4517+1_4518-1del
ENST00000422373.6:c.3160+2911_3160+2999del	ENSP00000416926.2:n.3160+2911_3160+2999de...
ENST00000610817.5:c.4655+1_4656-1del
ENST00000673639.2:c.279+6992_279+7080del
ENST00000676696.1:c.4877+1_4878-1del
ENST00000678304.1:n.148+645_148+733del
ENST00000344736.8:c.4598+1_4599-1del
ENST00000360319.8:c.4598+1_4599-1del
ENST00000369850.7:c.4598+1_4599-1del
ENST00000369856.7:c.4517+1_4518-1del
ENST00000420627.5:c.4554+1_4555-1del
ENST00000422373.5:c.4598+1_4599-1del
ENST00000466319.1:n.220+1_221-1del
ENST00000490936.5:n.611+1_612-1del
ENST00000610817.4:c.4517+1_4518-1del
NM_001110556.1:c.4598+1_4599-1del
NM_001456.3:c.4598+1_4599-1del
XM_011531127.1:c.4598+1_4599-1del
XM_011531128.1:c.4598+1_4599-1del
XM_011531129.1:c.4598+1_4599-1del
XM_011531130.1:c.4598+1_4599-1del
XM_011531131.1:c.4397+1_4398-1del
NM_001110556.2:c.4598+1_4599-1del
NM_001456.4:c.4598+1_4599-1del