Canonical Allele Identifier: CA2517878217
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153797_55153798insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAAGGAAATTTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC , CM000681.2:g.55153797_55153798insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAAGGAAATTTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC GRCh38
NC_000019.9:g.55665165_55665166insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAAGGAAATTTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC , CM000681.1:g.55665165_55665166insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAAGGAAATTTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC GRCh37
NC_000019.8:g.60356977_60356978insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAAGGAAATTTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC NCBI36
NG_007866.2:g.8980_8981insATTTCCTTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAA , LRG_432:g.8980_8981insATTTCCTTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAA
NG_011829.2:g.486_487insATTTCCTTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAA

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.549+277_549+278insATTTCCTTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAA MANE Select ENSP00000341838.5:n.549+277_549+278insATTTCCTTTTTTTTTTTTTTTGA...
ENST00000665070.1:c.582+277_582+278insATTTCCTTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAA ENSP00000499482.1:n.582+277_582+278insATTTCCTTTTTTTTTTTTTTTGA...
ENST00000344887.9:c.549+277_549+278insATTTCCTTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAA ENSP00000341838.5:n.549+277_549+278insATTTCCTTTTTTTTTTTTTTTGA...
ENST00000585806.5:n.548+277_548+278insATTTCCTTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAA
ENST00000588882.1:c.474+277_474+278insATTTCCTTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAA ENSP00000466729.1:n.474+277_474+278insATTTCCTTTTTTTTTTTTTTTGA...
ENST00000589864.1:n.377+277_377+278insATTTCCTTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAA
NM_000363.4:c.549+277_549+278insATTTCCTTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAA , LRG_432t1:c.549+277_549+278insATTTCCTTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAA NP_000354.4:n.549+277_549+278insATTTCCTTTTTTTTTTTTTTTGAGATGGA...
NM_000363.5:c.549+277_549+278insATTTCCTTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAA MANE Select NP_000354.4:n.549+277_549+278insATTTCCTTTTTTTTTTTTTTTGAGATGGA...