Canonical Allele Identifier: CA997258635
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153790_55153791insAAAAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGG , CM000681.2:g.55153790_55153791insAAAAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGG GRCh38
NC_000019.9:g.55665158_55665159insAAAAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGG , CM000681.1:g.55665158_55665159insAAAAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGG GRCh37
NC_000019.8:g.60356970_60356971insAAAAAGCAACTGCACCTGGACAGCAGAGACTCCATCTAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTTTAAACCTCAAAGATTACAGG NCBI36
NG_007866.2:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTTTTCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT , LRG_432:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTTTTCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT
NG_011829.2:g.483_484insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTTTTCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTTTTCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT MANE Select ENSP00000341838.5:n.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTT...
ENST00000665070.1:c.582+274_582+275insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTTTTCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT ENSP00000499482.1:n.582+274_582+275insAAATTTCCTTTTTTTTTTTTTTT...
ENST00000344887.9:c.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTTTTCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT ENSP00000341838.5:n.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTT...
ENST00000585806.5:n.548+274_548+275insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTTTTCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT
ENST00000588882.1:c.474+274_474+275insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTTTTCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT ENSP00000466729.1:n.474+274_474+275insAAATTTCCTTTTTTTTTTTTTTT...
ENST00000589864.1:n.377+274_377+275insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTTTTCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT
NM_000363.4:c.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTTTTCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT , LRG_432t1:c.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTTTTCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT NP_000354.4:n.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTTAGATGG...
NM_000363.5:c.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTTAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTTTTCCTGTAATCTTTGAGGTTTAAAAAAAATTTTTTTT MANE Select NP_000354.4:n.549+274_549+275insAAATTTCCTTTTTTTTTTTTTTTAGATGG...