Canonical Allele Identifier: CA997259386

Gene: TNNI3

Linked Data

• gnomAD v3: 19-55153755-A-AAAAAAAAATTTTTTTAAAACCTCAAAGATTACAGAAATAAGCAACTGCACCTGAACAGCAGAGACTCCATCAAAAAAAAAAAAAAAAGGAAATTT
• gnomAD v4: 19-55153755-A-AAAAAAAAATTTTTTTAAAACCTCAAAGATTACAGAAATAAGCAACTGCACCTGAACAGCAGAGACTCCATCAAAAAAAAAAAAAAAAGGAAATTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153770_55153771insAAAACCTCAAAGATTACAGAAATAAGCAACTGCACCTGAACAGCAGAGACTCCATCAAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTT , CM000681.2:g.55153770_55153771insAAAACCTCAAAGATTACAGAAATAAGCAACTGCACCTGAACAGCAGAGACTCCATCAAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTT	GRCh38
NC_000019.9:g.55665138_55665139insAAAACCTCAAAGATTACAGAAATAAGCAACTGCACCTGAACAGCAGAGACTCCATCAAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTT , CM000681.1:g.55665138_55665139insAAAACCTCAAAGATTACAGAAATAAGCAACTGCACCTGAACAGCAGAGACTCCATCAAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTT	GRCh37
NC_000019.8:g.60356950_60356951insAAAACCTCAAAGATTACAGAAATAAGCAACTGCACCTGAACAGCAGAGACTCCATCAAAAAAAAAAAAAAAAGGAAATTTAAAAAAAATTTTTTT	NCBI36
NG_007866.2:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTTTGATGGAGTCTCTGCTGTTCAGGTGCAGTTGCTTATTTCTGTAATCTTTGAGGTTTTAAAAAAATTTTTTTT , LRG_432:g.8977_8978insAAATTTCCTTTTTTTTTTTTTTTTGATGGAGTCTCTGCTGTTCAGGTGCAGTTGCTTATTTCTGTAATCTTTGAGGTTTTAAAAAAATTTTTTTT
NG_011829.2:g.483_484insAAATTTCCTTTTTTTTTTTTTTTTGATGGAGTCTCTGCTGTTCAGGTGCAGTTGCTTATTTCTGTAATCTTTGAGGTTTTAAAAAAATTTTTTTT

Transcript Alleles

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