Canonical Allele Identifier: CA997247018

Gene: TNNI3

Linked Data

• gnomAD v3: 19-55153733-A-AAAAAAAAAAAAAAAAGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTC
• gnomAD v4: 19-55153733-A-AAAAAAAAAAAAAAAAGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153747_55153748insAGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAA , CM000681.2:g.55153747_55153748insAGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAA	GRCh38
NC_000019.9:g.55665115_55665116insAGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAA , CM000681.1:g.55665115_55665116insAGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAA	GRCh37
NC_000019.8:g.60356927_60356928insAGAAATTAAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAA	NCBI36
NG_007866.2:g.8999_9000insGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCTTTTTTTTTTTTTTT , LRG_432:g.8999_9000insGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCTTTTTTTTTTTTTTT
NG_011829.2:g.505_506insGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.549+296_549+297insGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCTTTTTTTTTTTTTTT MANE Select	ENSP00000341838.5:n.549+296_549+297insGAGATGGAGTCTCTGCTGTCCAG...
ENST00000665070.1:c.582+296_582+297insGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCTTTTTTTTTTTTTTT	ENSP00000499482.1:n.582+296_582+297insGAGATGGAGTCTCTGCTGTCCAG...
ENST00000344887.9:c.549+296_549+297insGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCTTTTTTTTTTTTTTT	ENSP00000341838.5:n.549+296_549+297insGAGATGGAGTCTCTGCTGTCCAG...
ENST00000585806.5:n.548+296_548+297insGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCTTTTTTTTTTTTTTT
ENST00000588882.1:c.474+296_474+297insGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCTTTTTTTTTTTTTTT	ENSP00000466729.1:n.474+296_474+297insGAGATGGAGTCTCTGCTGTCCAG...
ENST00000589864.1:n.377+296_377+297insGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCTTTTTTTTTTTTTTT
NM_000363.4:c.549+296_549+297insGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCTTTTTTTTTTTTTTT , LRG_432t1:c.549+296_549+297insGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCTTTTTTTTTTTTTTT	NP_000354.4:n.549+296_549+297insGAGATGGAGTCTCTGCTGTCCAGGTGCAG...
NM_000363.5:c.549+296_549+297insGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTTAATTTCTTTTTTTTTTTTTTT MANE Select	NP_000354.4:n.549+296_549+297insGAGATGGAGTCTCTGCTGTCCAGGTGCAG...