Canonical Allele Identifier: CA997256232

Gene: TNNI3

Linked Data

• dbSNP Id: rs2085708350
• gnomAD v3: 19-55153755-A-AAAAAAAATTTTTTTTAAAACCTAAAAGATTACAGGCATAAGAAAATGAACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTT
• gnomAD v4: 19-55153755-A-AAAAAAAATTTTTTTTAAAACCTAAAAGATTACAGGCATAAGAAAATGAACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153762_55153763insTTTTTTTTAAAACCTAAAAGATTACAGGCATAAGAAAATGAACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAA , CM000681.2:g.55153762_55153763insTTTTTTTTAAAACCTAAAAGATTACAGGCATAAGAAAATGAACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAA	GRCh38
NC_000019.9:g.55665130_55665131insTTTTTTTTAAAACCTAAAAGATTACAGGCATAAGAAAATGAACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAA , CM000681.1:g.55665130_55665131insTTTTTTTTAAAACCTAAAAGATTACAGGCATAAGAAAATGAACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAA	GRCh37
NC_000019.8:g.60356942_60356943insTTTTTTTTAAAACCTAAAAGATTACAGGCATAAGAAAATGAACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAA	NCBI36
NG_007866.2:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTTCATTTTCTTATGCCTGTAATCTTTTAGGTTTTAAAAAAAATTTTTTT , LRG_432:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTTCATTTTCTTATGCCTGTAATCTTTTAGGTTTTAAAAAAAATTTTTTT
NG_011829.2:g.483_484insAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTTCATTTTCTTATGCCTGTAATCTTTTAGGTTTTAAAAAAAATTTTTTT

Transcript Alleles

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