Canonical Allele Identifier: CA997247111

Gene: TNNI3

Linked Data

• gnomAD v3: 19-55153752-A-ATTAAAAAAAATTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAAT
• gnomAD v4: 19-55153752-A-ATTAAAAAAAATTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153762_55153763insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAA , CM000681.2:g.55153762_55153763insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAA	GRCh38
NC_000019.9:g.55665130_55665131insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAA , CM000681.1:g.55665130_55665131insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAA	GRCh37
NC_000019.8:g.60356942_60356943insTTTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAA	NCBI36
NG_007866.2:g.8980_8981insATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTTTTAA , LRG_432:g.8980_8981insATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTTTTAA
NG_011829.2:g.486_487insATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTTTTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.549+277_549+278insATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTTTTAA MANE Select	ENSP00000341838.5:n.549+277_549+278insATTTCCTTTTTTTTTTTTTTGAG...
ENST00000665070.1:c.582+277_582+278insATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTTTTAA	ENSP00000499482.1:n.582+277_582+278insATTTCCTTTTTTTTTTTTTTGAG...
ENST00000344887.9:c.549+277_549+278insATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTTTTAA	ENSP00000341838.5:n.549+277_549+278insATTTCCTTTTTTTTTTTTTTGAG...
ENST00000585806.5:n.548+277_548+278insATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTTTTAA
ENST00000588882.1:c.474+277_474+278insATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTTTTAA	ENSP00000466729.1:n.474+277_474+278insATTTCCTTTTTTTTTTTTTTGAG...
ENST00000589864.1:n.377+277_377+278insATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTTTTAA
NM_000363.4:c.549+277_549+278insATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTTTTAA , LRG_432t1:c.549+277_549+278insATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTTTTAA	NP_000354.4:n.549+277_549+278insATTTCCTTTTTTTTTTTTTTGAGATGGAG...
NM_000363.5:c.549+277_549+278insATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAAATTTTTTTTAA MANE Select	NP_000354.4:n.549+277_549+278insATTTCCTTTTTTTTTTTTTTGAGATGGAG...