Canonical Allele Identifier: CA633870737

Gene: TNNI3

Linked Data

• dbSNP Id: rs1568857888
• gnomAD v2: 19-55665131-A-AAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAT
• gnomAD v3: 19-55153763-A-AAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAT
• gnomAD v4: 19-55153763-A-AAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAT
• MyVariant Identifiers: chr19:g.55665131_55665132insAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAT (hg19) ; chr19:g.55153763_55153764insAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153763_55153764insAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAT , CM000681.2:g.55153763_55153764insAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAT	GRCh38
NC_000019.9:g.55665131_55665132insAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAT , CM000681.1:g.55665131_55665132insAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAT	GRCh37
NC_000019.8:g.60356943_60356944insAACCTCAAAGATTACAGGCATAAGCAACTGCACCTGGACAGCAGAGACTCCATCTCAAAAAAAAAAAAAAGGAAATTTAAAAAAAT	NCBI36
NG_007866.2:g.8969_8970insATTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTT , LRG_432:g.8969_8970insATTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTT
NG_011829.2:g.475_476insATTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.549+266_549+267insATTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTT MANE Select	ENSP00000341838.5:n.549+266_549+267insATTTTTTTAAATTTCCTTTTTTT...
ENST00000665070.1:c.582+266_582+267insATTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTT	ENSP00000499482.1:n.582+266_582+267insATTTTTTTAAATTTCCTTTTTTT...
ENST00000344887.9:c.549+266_549+267insATTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTT	ENSP00000341838.5:n.549+266_549+267insATTTTTTTAAATTTCCTTTTTTT...
ENST00000585806.5:n.548+266_548+267insATTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTT
ENST00000588882.1:c.474+266_474+267insATTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTT	ENSP00000466729.1:n.474+266_474+267insATTTTTTTAAATTTCCTTTTTTT...
ENST00000589864.1:n.377+266_377+267insATTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTT
NM_000363.4:c.549+266_549+267insATTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTT , LRG_432t1:c.549+266_549+267insATTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTT	NP_000354.4:n.549+266_549+267insATTTTTTTAAATTTCCTTTTTTTTTTTTT...
NM_000363.5:c.549+266_549+267insATTTTTTTAAATTTCCTTTTTTTTTTTTTTGAGATGGAGTCTCTGCTGTCCAGGTGCAGTTGCTTATGCCTGTAATCTTTGAGGTT MANE Select	NP_000354.4:n.549+266_549+267insATTTTTTTAAATTTCCTTTTTTTTTTTTT...