Canonical Allele Identifier: CA997261153

Gene: TNNI3

Linked Data

• dbSNP Id: rs1568857870
• gnomAD v3: 19-55153756-A-AAAAAAATTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGAAAATTTT
• gnomAD v4: 19-55153756-A-AAAAAAATTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGAAAATTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153762_55153763insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGAAAATTTTAAAAAA , CM000681.2:g.55153762_55153763insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGAAAATTTTAAAAAA	GRCh38
NC_000019.9:g.55665130_55665131insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGAAAATTTTAAAAAA , CM000681.1:g.55665130_55665131insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGAAAATTTTAAAAAA	GRCh37
NC_000019.8:g.60356942_60356943insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGAAAATTTTAAAAAA	NCBI36
NG_007866.2:g.8976_8977insAAAATTTTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT , LRG_432:g.8976_8977insAAAATTTTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT
NG_011829.2:g.482_483insAAAATTTTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.549+273_549+274insAAAATTTTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT MANE Select	ENSP00000341838.5:n.549+273_549+274insAAAATTTTCTTTTTTTTTTTTTT...
ENST00000665070.1:c.582+273_582+274insAAAATTTTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT	ENSP00000499482.1:n.582+273_582+274insAAAATTTTCTTTTTTTTTTTTTT...
ENST00000344887.9:c.549+273_549+274insAAAATTTTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT	ENSP00000341838.5:n.549+273_549+274insAAAATTTTCTTTTTTTTTTTTTT...
ENST00000585806.5:n.548+273_548+274insAAAATTTTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT
ENST00000588882.1:c.474+273_474+274insAAAATTTTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT	ENSP00000466729.1:n.474+273_474+274insAAAATTTTCTTTTTTTTTTTTTT...
ENST00000589864.1:n.377+273_377+274insAAAATTTTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT
NM_000363.4:c.549+273_549+274insAAAATTTTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT , LRG_432t1:c.549+273_549+274insAAAATTTTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT	NP_000354.4:n.549+273_549+274insAAAATTTTCTTTTTTTTTTTTTTGAGATG...
NM_000363.5:c.549+273_549+274insAAAATTTTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT MANE Select	NP_000354.4:n.549+273_549+274insAAAATTTTCTTTTTTTTTTTTTTGAGATG...