Canonical Allele Identifier: CA2466655203
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154358382_154358386delinsTCAGA , CM000685.2:g.154358382_154358386delinsTCAGA GRCh38
NC_000023.10:g.153586750_153586754delinsTCAGA , CM000685.1:g.153586750_153586754delinsTCAGA GRCh37
NC_000023.9:g.153239944_153239948delinsTCAGA NCBI36
NG_011506.1:g.21253_21257delinsTCTGA
NG_011506.2:g.21253_21257delinsTCTGA

Transcript Alleles

HGVS Amino-acid change
ENST00000360319.9:c.4599-31_4599-27delinsTCTGA ENSP00000353467.4:n.4599-31_4599-27delins...
ENST00000369850.10:c.4599-31_4599-27delinsTCTGA MANE Select ENSP00000358866.3:n.4599-31_4599-27delins...
ENST00000369856.8:c.4518-31_4518-27delinsTCTGA ENSP00000358872.4:n.4518-31_4518-27delins...
ENST00000422373.6:c.3160+2969_3160+2973delinsTCTGA ENSP00000416926.2:n.3160+2969_3160+2973de...
ENST00000610817.5:c.4656-31_4656-27delinsTCTGA ENSP00000480593.2:n.4656-31_4656-27delins...
ENST00000673639.2:c.279+7050_279+7054delinsTCTGA
ENST00000676696.1:c.4878-31_4878-27delinsTCTGA ENSP00000503392.1:n.4878-31_4878-27delins...
ENST00000678304.1:n.148+703_148+707delinsTCTGA
ENST00000344736.8:c.4599-31_4599-27delinsTCTGA ENSP00000358863.3:n.4599-31_4599-27delins...
ENST00000360319.8:c.4599-31_4599-27delinsTCTGA ENSP00000353467.4:n.4599-31_4599-27delins...
ENST00000369850.7:c.4599-31_4599-27delinsTCTGA ENSP00000358866.3:n.4599-31_4599-27delins...
ENST00000369856.7:c.4518-31_4518-27delinsTCTGA ENSP00000358872.4:n.4518-31_4518-27delins...
ENST00000420627.5:c.4555-31_4555-27delinsTCTGA ENSP00000408921.1:n.4555-31_4555-27delins...
ENST00000422373.5:c.4599-31_4599-27delinsTCTGA ENSP00000416926.1:n.4599-31_4599-27delins...
ENST00000466319.1:n.221-31_221-27delinsTCTGA
ENST00000490936.5:n.612-31_612-27delinsTCTGA
ENST00000610817.4:c.4518-31_4518-27delinsTCTGA ENSP00000480593.1:n.4518-31_4518-27delins...
NM_001110556.1:c.4599-31_4599-27delinsTCTGA NP_001104026.1:n.4599-31_4599-27delinsTCT...
NM_001456.3:c.4599-31_4599-27delinsTCTGA NP_001447.2:n.4599-31_4599-27delinsTCTGA
XM_011531127.1:c.4599-31_4599-27delinsTCTGA XP_011529429.1:n.4599-31_4599-27delinsTCT...
XM_011531128.1:c.4599-31_4599-27delinsTCTGA XP_011529430.1:n.4599-31_4599-27delinsTCT...
XM_011531129.1:c.4599-31_4599-27delinsTCTGA XP_011529431.1:n.4599-31_4599-27delinsTCT...
XM_011531130.1:c.4599-31_4599-27delinsTCTGA XP_011529432.1:n.4599-31_4599-27delinsTCT...
XM_011531131.1:c.4398-31_4398-27delinsTCTGA XP_011529433.1:n.4398-31_4398-27delinsTCT...
NM_001110556.2:c.4599-31_4599-27delinsTCTGA MANE Select NP_001104026.1:n.4599-31_4599-27delinsTCT...
NM_001456.4:c.4599-31_4599-27delinsTCTGA NP_001447.2:n.4599-31_4599-27delinsTCTGA