Canonical Allele Identifier: CA997261225

Gene: TNNI3

Linked Data

• gnomAD v3: 19-55153775-C-CCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAAT
• gnomAD v4: 19-55153775-C-CCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153797_55153798insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAATCTCAAAGATTACAGGCATAAGC , CM000681.2:g.55153797_55153798insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAATCTCAAAGATTACAGGCATAAGC	GRCh38
NC_000019.9:g.55665165_55665166insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAATCTCAAAGATTACAGGCATAAGC , CM000681.1:g.55665165_55665166insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAATCTCAAAGATTACAGGCATAAGC	GRCh37
NC_000019.8:g.60356977_60356978insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAATCTCAAAGATTACAGGCATAAGC	NCBI36
NG_007866.2:g.8957_8958insATTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAG , LRG_432:g.8957_8958insATTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAG
NG_011829.2:g.463_464insATTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.549+254_549+255insATTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAG MANE Select	ENSP00000341838.5:n.549+254_549+255insATTTAAAAAAAATTTTTTTTAAA...
ENST00000665070.1:c.582+254_582+255insATTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAG	ENSP00000499482.1:n.582+254_582+255insATTTAAAAAAAATTTTTTTTAAA...
ENST00000344887.9:c.549+254_549+255insATTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAG	ENSP00000341838.5:n.549+254_549+255insATTTAAAAAAAATTTTTTTTAAA...
ENST00000585806.5:n.548+254_548+255insATTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAG
ENST00000588882.1:c.474+254_474+255insATTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAG	ENSP00000466729.1:n.474+254_474+255insATTTAAAAAAAATTTTTTTTAAA...
ENST00000589864.1:n.377+254_377+255insATTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAG
NM_000363.4:c.549+254_549+255insATTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAG , LRG_432t1:c.549+254_549+255insATTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAG	NP_000354.4:n.549+254_549+255insATTTAAAAAAAATTTTTTTTAAATTTCCT...
NM_000363.5:c.549+254_549+255insATTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAG MANE Select	NP_000354.4:n.549+254_549+255insATTTAAAAAAAATTTTTTTTAAATTTCCT...