Canonical Allele Identifier: CA2814881069
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153797_55153798insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAACGGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC , CM000681.2:g.55153797_55153798insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAACGGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC GRCh38
NC_000019.9:g.55665165_55665166insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAACGGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC , CM000681.1:g.55665165_55665166insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAACGGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC GRCh37
NC_000019.8:g.60356977_60356978insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAACGGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC NCBI36
NG_007866.2:g.8985_8986insGTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCC , LRG_432:g.8985_8986insGTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCC
NG_011829.2:g.491_492insGTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.549+282_549+283insGTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCC MANE Select ENSP00000341838.5:n.549+282_549+283insGTTTTTTTTTTTTTTGAGATGGA...
ENST00000665070.1:c.582+282_582+283insGTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCC ENSP00000499482.1:n.582+282_582+283insGTTTTTTTTTTTTTTGAGATGGA...
ENST00000344887.9:c.549+282_549+283insGTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCC ENSP00000341838.5:n.549+282_549+283insGTTTTTTTTTTTTTTGAGATGGA...
ENST00000585806.5:n.548+282_548+283insGTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCC
ENST00000588882.1:c.474+282_474+283insGTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCC ENSP00000466729.1:n.474+282_474+283insGTTTTTTTTTTTTTTGAGATGGA...
ENST00000589864.1:n.377+282_377+283insGTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCC
NM_000363.4:c.549+282_549+283insGTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCC , LRG_432t1:c.549+282_549+283insGTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCC NP_000354.4:n.549+282_549+283insGTTTTTTTTTTTTTTGAGATGGAGTCTCT...
NM_000363.5:c.549+282_549+283insGTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCC MANE Select NP_000354.4:n.549+282_549+283insGTTTTTTTTTTTTTTGAGATGGAGTCTCT...