Canonical Allele Identifier: CA633870728

Gene: TNNI3

Linked Data

• dbSNP Id: rs1568857870
• gnomAD v2: 19-55665124-A-AAAAAAATTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTT
• gnomAD v3: 19-55153756-A-AAAAAAATTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTT
• gnomAD v4: 19-55153756-A-AAAAAAATTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTT
• MyVariant Identifiers: chr19:g.55665124_55665125insAAAAAATTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTT (hg19) ; chr19:g.55153756_55153757insAAAAAATTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153762_55153763insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTTAAAAAA , CM000681.2:g.55153762_55153763insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTTAAAAAA	GRCh38
NC_000019.9:g.55665130_55665131insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTTAAAAAA , CM000681.1:g.55665130_55665131insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTTAAAAAA	GRCh37
NC_000019.8:g.60356942_60356943insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTTAAAAAA	NCBI36
NG_007866.2:g.8976_8977insAAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT , LRG_432:g.8976_8977insAAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT
NG_011829.2:g.482_483insAAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTT

Transcript Alleles

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