Canonical Allele Identifier: CA997261282
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153800_55153801insCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGCCCC , CM000681.2:g.55153800_55153801insCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGCCCC GRCh38
NC_000019.9:g.55665168_55665169insCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGCCCC , CM000681.1:g.55665168_55665169insCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGCCCC GRCh37
NC_000019.8:g.60356980_60356981insCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGGCATAAGCCCC NCBI36
NG_007866.2:g.8933_8934insGGGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGG , LRG_432:g.8933_8934insGGGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGG
NG_011829.2:g.439_440insGGGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.549+230_549+231insGGGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGG MANE Select ENSP00000341838.5:n.549+230_549+231insGGGCTTATGCCTGTAATCTTTGA...
ENST00000665070.1:c.582+230_582+231insGGGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGG ENSP00000499482.1:n.582+230_582+231insGGGCTTATGCCTGTAATCTTTGA...
ENST00000344887.9:c.549+230_549+231insGGGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGG ENSP00000341838.5:n.549+230_549+231insGGGCTTATGCCTGTAATCTTTGA...
ENST00000585806.5:n.548+230_548+231insGGGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGG
ENST00000588882.1:c.474+230_474+231insGGGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGG ENSP00000466729.1:n.474+230_474+231insGGGCTTATGCCTGTAATCTTTGA...
ENST00000589864.1:n.377+230_377+231insGGGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGG
NM_000363.4:c.549+230_549+231insGGGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGG , LRG_432t1:c.549+230_549+231insGGGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGG NP_000354.4:n.549+230_549+231insGGGCTTATGCCTGTAATCTTTGAGGTTTA...
NM_000363.5:c.549+230_549+231insGGGCTTATGCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGG MANE Select NP_000354.4:n.549+230_549+231insGGGCTTATGCCTGTAATCTTTGAGGTTTA...