Canonical Allele Identifier: CA997258800
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153796_55153797insAAAATGCCCCTGGACAGCAGAGACTCCATCACAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAG , CM000681.2:g.55153796_55153797insAAAATGCCCCTGGACAGCAGAGACTCCATCACAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAG GRCh38
NC_000019.9:g.55665164_55665165insAAAATGCCCCTGGACAGCAGAGACTCCATCACAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAG , CM000681.1:g.55665164_55665165insAAAATGCCCCTGGACAGCAGAGACTCCATCACAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAG GRCh37
NC_000019.8:g.60356976_60356977insAAAATGCCCCTGGACAGCAGAGACTCCATCACAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAG NCBI36
NG_007866.2:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTGTGATGGAGTCTCTGCTGTCCAGGGGCATTTTCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT , LRG_432:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTGTGATGGAGTCTCTGCTGTCCAGGGGCATTTTCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT
NG_011829.2:g.483_484insAAATTTCCTTTTTTTTTTTTTTGTGATGGAGTCTCTGCTGTCCAGGGGCATTTTCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT

Transcript Alleles

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