Canonical Allele Identifier: CA2814881047
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153797_55153798insAACTGCACCTGGACAGCATATACTCCATCTCAAAAAAAAAAAAAAAGGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC , CM000681.2:g.55153797_55153798insAACTGCACCTGGACAGCATATACTCCATCTCAAAAAAAAAAAAAAAGGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC GRCh38
NC_000019.9:g.55665165_55665166insAACTGCACCTGGACAGCATATACTCCATCTCAAAAAAAAAAAAAAAGGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC , CM000681.1:g.55665165_55665166insAACTGCACCTGGACAGCATATACTCCATCTCAAAAAAAAAAAAAAAGGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC GRCh37
NC_000019.8:g.60356977_60356978insAACTGCACCTGGACAGCATATACTCCATCTCAAAAAAAAAAAAAAAGGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC NCBI36
NG_007866.2:g.9000_9001insGAGATGGAGTATATGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCCTTTTTTTTTTTTTTT , LRG_432:g.9000_9001insGAGATGGAGTATATGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCCTTTTTTTTTTTTTTT
NG_011829.2:g.506_507insGAGATGGAGTATATGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCCTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.549+297_549+298insGAGATGGAGTATATGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCCTTTTTTTTTTTTTTT MANE Select ENSP00000341838.5:n.549+297_549+298insGAGATGGAGTATATGCTGTCCAG...
ENST00000665070.1:c.582+297_582+298insGAGATGGAGTATATGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCCTTTTTTTTTTTTTTT ENSP00000499482.1:n.582+297_582+298insGAGATGGAGTATATGCTGTCCAG...
ENST00000344887.9:c.549+297_549+298insGAGATGGAGTATATGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCCTTTTTTTTTTTTTTT ENSP00000341838.5:n.549+297_549+298insGAGATGGAGTATATGCTGTCCAG...
ENST00000585806.5:n.548+297_548+298insGAGATGGAGTATATGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCCTTTTTTTTTTTTTTT
ENST00000588882.1:c.474+297_474+298insGAGATGGAGTATATGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCCTTTTTTTTTTTTTTT ENSP00000466729.1:n.474+297_474+298insGAGATGGAGTATATGCTGTCCAG...
ENST00000589864.1:n.377+297_377+298insGAGATGGAGTATATGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCCTTTTTTTTTTTTTTT
NM_000363.4:c.549+297_549+298insGAGATGGAGTATATGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCCTTTTTTTTTTTTTTT , LRG_432t1:c.549+297_549+298insGAGATGGAGTATATGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCCTTTTTTTTTTTTTTT NP_000354.4:n.549+297_549+298insGAGATGGAGTATATGCTGTCCAGGTGCAG...
NM_000363.5:c.549+297_549+298insGAGATGGAGTATATGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCCTTTTTTTTTTTTTTT MANE Select NP_000354.4:n.549+297_549+298insGAGATGGAGTATATGCTGTCCAGGTGCAG...