Canonical Allele Identifier: CA997261188

Gene: TNNI3

Linked Data

• gnomAD v3: 19-55153756-A-AAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAGGAAATTTT
• gnomAD v4: 19-55153756-A-AAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAGGAAATTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153797_55153798insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAGGAAATTTTAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC , CM000681.2:g.55153797_55153798insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAGGAAATTTTAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC	GRCh38
NC_000019.9:g.55665165_55665166insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAGGAAATTTTAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC , CM000681.1:g.55665165_55665166insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAGGAAATTTTAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC	GRCh37
NC_000019.8:g.60356977_60356978insAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAGGAAATTTTAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGC	NCBI36
NG_007866.2:g.8976_8977insAAAATTTCCTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTT , LRG_432:g.8976_8977insAAAATTTCCTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTT
NG_011829.2:g.482_483insAAAATTTCCTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.549+273_549+274insAAAATTTCCTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTT MANE Select	ENSP00000341838.5:n.549+273_549+274insAAAATTTCCTTTTTTTTTTTTTG...
ENST00000665070.1:c.582+273_582+274insAAAATTTCCTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTT	ENSP00000499482.1:n.582+273_582+274insAAAATTTCCTTTTTTTTTTTTTG...
ENST00000344887.9:c.549+273_549+274insAAAATTTCCTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTT	ENSP00000341838.5:n.549+273_549+274insAAAATTTCCTTTTTTTTTTTTTG...
ENST00000585806.5:n.548+273_548+274insAAAATTTCCTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTT
ENST00000588882.1:c.474+273_474+274insAAAATTTCCTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTT	ENSP00000466729.1:n.474+273_474+274insAAAATTTCCTTTTTTTTTTTTTG...
ENST00000589864.1:n.377+273_377+274insAAAATTTCCTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTT
NM_000363.4:c.549+273_549+274insAAAATTTCCTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTT , LRG_432t1:c.549+273_549+274insAAAATTTCCTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTT	NP_000354.4:n.549+273_549+274insAAAATTTCCTTTTTTTTTTTTTGAGATGG...
NM_000363.5:c.549+273_549+274insAAAATTTCCTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTT MANE Select	NP_000354.4:n.549+273_549+274insAAAATTTCCTTTTTTTTTTTTTGAGATGG...