Canonical Allele Identifier: CA2814881286

Gene: TNNI3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153798_55153799insTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTCAACCTCAAAGATTACAGGCATAAGCA , CM000681.2:g.55153798_55153799insTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTCAACCTCAAAGATTACAGGCATAAGCA	GRCh38
NC_000019.9:g.55665166_55665167insTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTCAACCTCAAAGATTACAGGCATAAGCA , CM000681.1:g.55665166_55665167insTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTCAACCTCAAAGATTACAGGCATAAGCA	GRCh37
NC_000019.8:g.60356978_60356979insTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTCAACCTCAAAGATTACAGGCATAAGCA	NCBI36
NG_007866.2:g.8934_8935insTGCTTATGCCTGTAATCTTTGAGGTTGAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCA , LRG_432:g.8934_8935insTGCTTATGCCTGTAATCTTTGAGGTTGAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCA
NG_011829.2:g.440_441insTGCTTATGCCTGTAATCTTTGAGGTTGAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.549+231_549+232insTGCTTATGCCTGTAATCTTTGAGGTTGAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCA MANE Select	ENSP00000341838.5:n.549+231_549+232insTGCTTATGCCTGTAATCTTTGAG...
ENST00000665070.1:c.582+231_582+232insTGCTTATGCCTGTAATCTTTGAGGTTGAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCA	ENSP00000499482.1:n.582+231_582+232insTGCTTATGCCTGTAATCTTTGAG...
ENST00000344887.9:c.549+231_549+232insTGCTTATGCCTGTAATCTTTGAGGTTGAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCA	ENSP00000341838.5:n.549+231_549+232insTGCTTATGCCTGTAATCTTTGAG...
ENST00000585806.5:n.548+231_548+232insTGCTTATGCCTGTAATCTTTGAGGTTGAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCA
ENST00000588882.1:c.474+231_474+232insTGCTTATGCCTGTAATCTTTGAGGTTGAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCA	ENSP00000466729.1:n.474+231_474+232insTGCTTATGCCTGTAATCTTTGAG...
ENST00000589864.1:n.377+231_377+232insTGCTTATGCCTGTAATCTTTGAGGTTGAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCA
NM_000363.4:c.549+231_549+232insTGCTTATGCCTGTAATCTTTGAGGTTGAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCA , LRG_432t1:c.549+231_549+232insTGCTTATGCCTGTAATCTTTGAGGTTGAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCA	NP_000354.4:n.549+231_549+232insTGCTTATGCCTGTAATCTTTGAGGTTGAA...
NM_000363.5:c.549+231_549+232insTGCTTATGCCTGTAATCTTTGAGGTTGAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCA MANE Select	NP_000354.4:n.549+231_549+232insTGCTTATGCCTGTAATCTTTGAGGTTGAA...