Canonical Allele Identifier: CA997259044

Gene: TNNI3

Linked Data

• dbSNP Id: rs2085708723
• gnomAD v3: 19-55153755-A-AAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCAAAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTT
• gnomAD v4: 19-55153755-A-AAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCAAAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153792_55153793insAAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCA , CM000681.2:g.55153792_55153793insAAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCA	GRCh38
NC_000019.9:g.55665160_55665161insAAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCA , CM000681.1:g.55665160_55665161insAAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCA	GRCh37
NC_000019.8:g.60356972_60356973insAAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCA	NCBI36
NG_007866.2:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTTTGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT , LRG_432:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTTTGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT
NG_011829.2:g.483_484insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTTTGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT

Transcript Alleles

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