Canonical Allele Identifier: CA2533505195
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153800_55153801insCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGCCATATTCCCC , CM000681.2:g.55153800_55153801insCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGCCATATTCCCC GRCh38
NC_000019.9:g.55665168_55665169insCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGCCATATTCCCC , CM000681.1:g.55665168_55665169insCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGCCATATTCCCC GRCh37
NC_000019.8:g.60356980_60356981insCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGCCATATTCCCC NCBI36
NG_007866.2:g.8933_8934insGGGAATATGGCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGG , LRG_432:g.8933_8934insGGGAATATGGCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGG
NG_011829.2:g.439_440insGGGAATATGGCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGG

Transcript Alleles

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