Canonical Allele Identifier: CA997261159
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153762_55153763insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAGGAAATTTTAAAAAA , CM000681.2:g.55153762_55153763insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAGGAAATTTTAAAAAA GRCh38
NC_000019.9:g.55665130_55665131insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAGGAAATTTTAAAAAA , CM000681.1:g.55665130_55665131insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAGGAAATTTTAAAAAA GRCh37
NC_000019.8:g.60356942_60356943insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAGGAAATTTTAAAAAA NCBI36
NG_007866.2:g.8976_8977insAAAATTTCCTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT , LRG_432:g.8976_8977insAAAATTTCCTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT
NG_011829.2:g.482_483insAAAATTTCCTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.549+273_549+274insAAAATTTCCTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT MANE Select ENSP00000341838.5:n.549+273_549+274insAAAATTTCCTTTTTTTTTTTGAG...
ENST00000665070.1:c.582+273_582+274insAAAATTTCCTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT ENSP00000499482.1:n.582+273_582+274insAAAATTTCCTTTTTTTTTTTGAG...
ENST00000344887.9:c.549+273_549+274insAAAATTTCCTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT ENSP00000341838.5:n.549+273_549+274insAAAATTTCCTTTTTTTTTTTGAG...
ENST00000585806.5:n.548+273_548+274insAAAATTTCCTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT
ENST00000588882.1:c.474+273_474+274insAAAATTTCCTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT ENSP00000466729.1:n.474+273_474+274insAAAATTTCCTTTTTTTTTTTGAG...
ENST00000589864.1:n.377+273_377+274insAAAATTTCCTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT
NM_000363.4:c.549+273_549+274insAAAATTTCCTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT , LRG_432t1:c.549+273_549+274insAAAATTTCCTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT NP_000354.4:n.549+273_549+274insAAAATTTCCTTTTTTTTTTTGAGATGGAG...
NM_000363.5:c.549+273_549+274insAAAATTTCCTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT MANE Select NP_000354.4:n.549+273_549+274insAAAATTTCCTTTTTTTTTTTGAGATGGAG...