Canonical Allele Identifier: CA997261167

Gene: TNNI3

Linked Data

• dbSNP Id: rs2085708902
• gnomAD v3: 19-55153756-A-AAAAAATTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTT
• gnomAD v4: 19-55153756-A-AAAAAATTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153761_55153762insTTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTTAAAAA , CM000681.2:g.55153761_55153762insTTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTTAAAAA	GRCh38
NC_000019.9:g.55665129_55665130insTTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTTAAAAA , CM000681.1:g.55665129_55665130insTTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTTAAAAA	GRCh37
NC_000019.8:g.60356941_60356942insTTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTTAAAAA	NCBI36
NG_007866.2:g.8976_8977insAAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAAATTTTT , LRG_432:g.8976_8977insAAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAAATTTTT
NG_011829.2:g.482_483insAAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAAATTTTT

Transcript Alleles

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