Canonical Allele Identifier: CA2552220195

Gene: TNNI3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153797_55153798insAACTGCACATGGACAGCAGAGACTCCTGCTCCAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC , CM000681.2:g.55153797_55153798insAACTGCACATGGACAGCAGAGACTCCTGCTCCAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC	GRCh38
NC_000019.9:g.55665165_55665166insAACTGCACATGGACAGCAGAGACTCCTGCTCCAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC , CM000681.1:g.55665165_55665166insAACTGCACATGGACAGCAGAGACTCCTGCTCCAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC	GRCh37
NC_000019.8:g.60356977_60356978insAACTGCACATGGACAGCAGAGACTCCTGCTCCAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC	NCBI36
NG_007866.2:g.8977_8978insAAATTTCCTTTTTTTTTTTTTGGAGCAGGAGTCTCTGCTGTCCATGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT , LRG_432:g.8977_8978insAAATTTCCTTTTTTTTTTTTTGGAGCAGGAGTCTCTGCTGTCCATGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT
NG_011829.2:g.483_484insAAATTTCCTTTTTTTTTTTTTGGAGCAGGAGTCTCTGCTGTCCATGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT

Transcript Alleles

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