Canonical Allele Identifier: CA997256936

Gene: TNNI3

Linked Data

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

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153797_55153798insAACTGCACCTGGACAGGAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC , CM000681.2:g.55153797_55153798insAACTGCACCTGGACAGGAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC	GRCh38
NC_000019.9:g.55665165_55665166insAACTGCACCTGGACAGGAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC , CM000681.1:g.55665165_55665166insAACTGCACCTGGACAGGAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC	GRCh37
NC_000019.8:g.60356977_60356978insAACTGCACCTGGACAGGAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC	NCBI36
NG_007866.2:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTCCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT , LRG_432:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTCCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT
NG_011829.2:g.483_484insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTCCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT

Transcript Alleles

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