Canonical Allele Identifier: CA997259813

Gene: TNNI3

Linked Data

• gnomAD v3: 19-55153755-A-AAAAAAAAATTTTTTTTAAACCTAAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTT
• gnomAD v4: 19-55153755-A-AAAAAAAAATTTTTTTTAAACCTAAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153777_55153778insAAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCT , CM000681.2:g.55153777_55153778insAAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCT	GRCh38
NC_000019.9:g.55665145_55665146insAAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCT , CM000681.1:g.55665145_55665146insAAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCT	GRCh37
NC_000019.8:g.60356957_60356958insAAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCT	NCBI36
NG_007866.2:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTTAGGTTTAAAAAAAATTTTTTTT , LRG_432:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTTAGGTTTAAAAAAAATTTTTTTT
NG_011829.2:g.483_484insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTTAGGTTTAAAAAAAATTTTTTTT

Transcript Alleles

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