Canonical Allele Identifier: CA997247068

Gene: TNNI3

Linked Data

• gnomAD v3: 19-55153749-G-GAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGA
• gnomAD v4: 19-55153749-G-GAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153797_55153798insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGAAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC , CM000681.2:g.55153797_55153798insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGAAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC	GRCh38
NC_000019.9:g.55665165_55665166insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGAAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC , CM000681.1:g.55665165_55665166insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGAAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC	GRCh37
NC_000019.8:g.60356977_60356978insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGAAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC	NCBI36
NG_007866.2:g.8983_8984insTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTT , LRG_432:g.8983_8984insTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTT
NG_011829.2:g.489_490insTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.549+280_549+281insTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTT MANE Select	ENSP00000341838.5:n.549+280_549+281insTCTTTTTTTTTTTTTTGAGATGG...
ENST00000665070.1:c.582+280_582+281insTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTT	ENSP00000499482.1:n.582+280_582+281insTCTTTTTTTTTTTTTTGAGATGG...
ENST00000344887.9:c.549+280_549+281insTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTT	ENSP00000341838.5:n.549+280_549+281insTCTTTTTTTTTTTTTTGAGATGG...
ENST00000585806.5:n.548+280_548+281insTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTT
ENST00000588882.1:c.474+280_474+281insTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTT	ENSP00000466729.1:n.474+280_474+281insTCTTTTTTTTTTTTTTGAGATGG...
ENST00000589864.1:n.377+280_377+281insTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTT
NM_000363.4:c.549+280_549+281insTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTT , LRG_432t1:c.549+280_549+281insTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTT	NP_000354.4:n.549+280_549+281insTCTTTTTTTTTTTTTTGAGATGGAGTCTC...
NM_000363.5:c.549+280_549+281insTCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTT MANE Select	NP_000354.4:n.549+280_549+281insTCTTTTTTTTTTTTTTGAGATGGAGTCTC...