Canonical Allele Identifier: CA2547560726
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153789_55153790insACATAAGCAACTGCACCTAGACAGAAAAAACTCCACCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAG , CM000681.2:g.55153789_55153790insACATAAGCAACTGCACCTAGACAGAAAAAACTCCACCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAG GRCh38
NC_000019.9:g.55665157_55665158insACATAAGCAACTGCACCTAGACAGAAAAAACTCCACCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAG , CM000681.1:g.55665157_55665158insACATAAGCAACTGCACCTAGACAGAAAAAACTCCACCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAG GRCh37
NC_000019.8:g.60356969_60356970insACATAAGCAACTGCACCTAGACAGAAAAAACTCCACCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAG NCBI36
NG_007866.2:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTGAGGTGGAGTTTTTTCTGTCTAGGTGCAGTTGCTTATGTCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT , LRG_432:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTGAGGTGGAGTTTTTTCTGTCTAGGTGCAGTTGCTTATGTCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT
NG_011829.2:g.483_484insAAATTTCCTTTTTTTTTTTTTTGAGGTGGAGTTTTTTCTGTCTAGGTGCAGTTGCTTATGTCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTGAGGTGGAGTTTTTTCTGTCTAGGTGCAGTTGCTTATGTCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT MANE Select ENSP00000341838.5:n.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTG...
ENST00000665070.1:c.582+274_582+275insAAATTTCCTTTTTTTTTTTTTTGAGGTGGAGTTTTTTCTGTCTAGGTGCAGTTGCTTATGTCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT ENSP00000499482.1:n.582+274_582+275insAAATTTCCTTTTTTTTTTTTTTG...
ENST00000344887.9:c.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTGAGGTGGAGTTTTTTCTGTCTAGGTGCAGTTGCTTATGTCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT ENSP00000341838.5:n.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTG...
ENST00000585806.5:n.548+274_548+275insAAATTTCCTTTTTTTTTTTTTTGAGGTGGAGTTTTTTCTGTCTAGGTGCAGTTGCTTATGTCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT
ENST00000588882.1:c.474+274_474+275insAAATTTCCTTTTTTTTTTTTTTGAGGTGGAGTTTTTTCTGTCTAGGTGCAGTTGCTTATGTCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT ENSP00000466729.1:n.474+274_474+275insAAATTTCCTTTTTTTTTTTTTTG...
ENST00000589864.1:n.377+274_377+275insAAATTTCCTTTTTTTTTTTTTTGAGGTGGAGTTTTTTCTGTCTAGGTGCAGTTGCTTATGTCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT
NM_000363.4:c.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTGAGGTGGAGTTTTTTCTGTCTAGGTGCAGTTGCTTATGTCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT , LRG_432t1:c.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTGAGGTGGAGTTTTTTCTGTCTAGGTGCAGTTGCTTATGTCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT NP_000354.4:n.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTGAGGTGG...
NM_000363.5:c.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTGAGGTGGAGTTTTTTCTGTCTAGGTGCAGTTGCTTATGTCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT MANE Select NP_000354.4:n.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTGAGGTGG...