Canonical Allele Identifier: CA2540410597
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153770_55153771insAAAACCTAAAAGATTACAGGCATAAGAAACTGCACCTGGAAAGCAGAGACTCAATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTT , CM000681.2:g.55153770_55153771insAAAACCTAAAAGATTACAGGCATAAGAAACTGCACCTGGAAAGCAGAGACTCAATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTT GRCh38
NC_000019.9:g.55665138_55665139insAAAACCTAAAAGATTACAGGCATAAGAAACTGCACCTGGAAAGCAGAGACTCAATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTT , CM000681.1:g.55665138_55665139insAAAACCTAAAAGATTACAGGCATAAGAAACTGCACCTGGAAAGCAGAGACTCAATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTT GRCh37
NC_000019.8:g.60356950_60356951insAAAACCTAAAAGATTACAGGCATAAGAAACTGCACCTGGAAAGCAGAGACTCAATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTT NCBI36
NG_007866.2:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTTAGATTGAGTCTCTGCTTTCCAGGTGCAGTTTCTTATGCCTGTAATCTTTTAGGTTTTAAAAAAATTTTTTTT , LRG_432:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTTAGATTGAGTCTCTGCTTTCCAGGTGCAGTTTCTTATGCCTGTAATCTTTTAGGTTTTAAAAAAATTTTTTTT
NG_011829.2:g.483_484insAAATTTCCTTTTTTTTTTTTTTTAGATTGAGTCTCTGCTTTCCAGGTGCAGTTTCTTATGCCTGTAATCTTTTAGGTTTTAAAAAAATTTTTTTT

Transcript Alleles

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