Canonical Allele Identifier: CA997255824

Gene: TNNI3

Linked Data

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

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153785_55153786insGCAGGCATAAGCAACTGCGCCTGGACAGCAGAGACTCAATCAAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATT , CM000681.2:g.55153785_55153786insGCAGGCATAAGCAACTGCGCCTGGACAGCAGAGACTCAATCAAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATT	GRCh38
NC_000019.9:g.55665153_55665154insGCAGGCATAAGCAACTGCGCCTGGACAGCAGAGACTCAATCAAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATT , CM000681.1:g.55665153_55665154insGCAGGCATAAGCAACTGCGCCTGGACAGCAGAGACTCAATCAAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATT	GRCh37
NC_000019.8:g.60356965_60356966insGCAGGCATAAGCAACTGCGCCTGGACAGCAGAGACTCAATCAAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATT	NCBI36
NG_007866.2:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTTTGATTGAGTCTCTGCTGTCCAGGCGCAGTTGCTTATGCCTGCAATCTTTGAGGTTTAAAAAAAATTTTTTTT , LRG_432:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTTTGATTGAGTCTCTGCTGTCCAGGCGCAGTTGCTTATGCCTGCAATCTTTGAGGTTTAAAAAAAATTTTTTTT
NG_011829.2:g.483_484insAAATTTCCTTTTTTTTTTTTTTTTGATTGAGTCTCTGCTGTCCAGGCGCAGTTGCTTATGCCTGCAATCTTTGAGGTTTAAAAAAAATTTTTTTT

Transcript Alleles

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