Canonical Allele Identifier: CA090359
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 654045
dbSNP Id: rs560019679

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201365229del , CM000663.2:g.201365229del GRCh38
NC_000001.10:g.201334357del , CM000663.1:g.201334357del GRCh37
NC_000001.9:g.199600980del NCBI36
NG_007556.1:g.17451del

Transcript Alleles

HGVS Amino-acid Change
ENST00000455702.7:c.360del ENSP00000402238.3:p.Glu121ArgfsTer?
ENST00000367318.10:c.345del ENSP00000356287.5:p.Glu116ArgfsTer?
ENST00000367322.6:c.342del ENSP00000356291.2:p.Glu115ArgfsTer?
ENST00000412633.3:c.345del ENSP00000408731.2:p.Glu116ArgfsTer?
ENST00000422165.6:c.375del ENSP00000395163.2:p.Glu126ArgfsTer?
ENST00000438742.6:c.327del ENSP00000414036.2:p.Glu110ArgfsTer?
ENST00000455702.6:c.360del ENSP00000402238.2:p.Glu121ArgfsTer?
ENST00000651504.1:n.839del
ENST00000656932.1:c.375del MANE Select ENSP00000499593.1:p.Glu126ArgfsTer?
ENST00000658476.1:c.345del ENSP00000499741.1:p.Glu116ArgfsTer?
ENST00000660295.1:c.345del ENSP00000499418.1:p.Glu116ArgfsTer?
ENST00000662159.1:c.162+2551del ENSP00000499796.1:n.162+2551del
ENST00000663843.1:c.*275del ENSP00000499590.1:n.*275del
ENST00000666449.1:c.345del ENSP00000499667.1:p.Glu116ArgfsTer?
ENST00000236918.11:c.375del ENSP00000236918.8:p.Glu126ArgfsTer?
ENST00000360372.8:c.291+383del ENSP00000353535.5:n.291+383del
ENST00000367315.6:c.351del ENSP00000356284.3:p.Glu118ArgfsTer?
ENST00000367317.8:c.330del ENSP00000356286.5:p.Glu111ArgfsTer?
ENST00000367318.9:c.345del ENSP00000356287.5:p.Glu116ArgfsTer?
ENST00000367320.6:c.291+383del ENSP00000356289.2:n.291+383del
ENST00000367322.5:c.345del ENSP00000356291.1:p.Glu116ArgfsTer?
ENST00000421663.6:c.168del ENSP00000404134.3:p.Glu57ArgfsTer?
ENST00000438742.5:c.330del ENSP00000414036.1:p.Glu111ArgfsTer?
ENST00000455702.5:c.375del ENSP00000402238.1:p.Glu126ArgfsTer?
ENST00000458432.6:c.168del ENSP00000387874.3:p.Glu57ArgfsTer?
ENST00000466570.5:n.601del
ENST00000491504.5:n.1584del
ENST00000503459.1:n.214del
ENST00000509001.5:c.345del ENSP00000422031.1:p.Glu116ArgfsTer?
ENST00000515042.5:n.271del
NM_000364.3:c.375del NP_000355.2:p.Glu126ArgfsTer?
NM_001001430.2:c.345del NP_001001430.1:p.Glu116ArgfsTer?
NM_001001431.2:c.345del NP_001001431.1:p.Glu116ArgfsTer?
NM_001001432.2:c.330del NP_001001432.1:p.Glu111ArgfsTer?
NM_001276345.1:c.375del NP_001263274.1:p.Glu126ArgfsTer?
NM_001276346.1:c.291+383del NP_001263275.1:n.291+383del
NM_001276347.1:c.345del NP_001263276.1:p.Glu116ArgfsTer?
XM_006711508.2:c.345del XP_006711571.1:p.Glu116ArgfsTer?
XM_006711509.2:c.342del XP_006711572.1:p.Glu115ArgfsTer?
XM_011509938.1:c.375del XP_011508240.1:p.Glu126ArgfsTer?
XM_011509939.1:c.372del XP_011508241.1:p.Glu125ArgfsTer?
XM_011509940.1:c.375del XP_011508242.1:p.Glu126ArgfsTer?
XM_011509941.1:c.372del XP_011508243.1:p.Glu125ArgfsTer?
XM_011509942.1:c.330del XP_011508244.1:p.Glu111ArgfsTer?
XM_011509943.1:c.330del XP_011508245.1:p.Glu111ArgfsTer?
XM_011509944.1:c.327del XP_011508246.1:p.Glu110ArgfsTer?
XM_011509945.1:c.375del XP_011508247.1:p.Glu126ArgfsTer?
XM_011509946.1:c.168del XP_011508248.1:p.Glu57ArgfsTer?
XM_006711508.3:c.345del XP_006711571.1:p.Glu116ArgfsTer?
XM_006711509.3:c.342del XP_006711572.1:p.Glu115ArgfsTer?
XM_011509938.2:c.375del XP_011508240.1:p.Glu126ArgfsTer?
XM_011509940.2:c.375del XP_011508242.1:p.Glu126ArgfsTer?
XM_011509941.2:c.372del XP_011508243.1:p.Glu125ArgfsTer?
XM_011509942.2:c.330del XP_011508244.1:p.Glu111ArgfsTer?
XM_011509943.2:c.330del XP_011508245.1:p.Glu111ArgfsTer?
XM_011509944.2:c.327del XP_011508246.1:p.Glu110ArgfsTer?
XM_017002216.2:c.345del XP_016857705.1:p.Glu116ArgfsTer?
XM_017002217.1:c.345del XP_016857706.1:p.Glu116ArgfsTer?
XM_024449450.1:c.375del XP_024305218.1:p.Glu126ArgfsTer?
XM_024449454.1:c.342del XP_024305222.1:p.Glu115ArgfsTer?
XM_024449455.1:c.345del XP_024305223.1:p.Glu116ArgfsTer?
NM_000364.4:c.375del NP_000355.2:p.Glu126ArgfsTer?
NM_001001430.3:c.345del NP_001001430.1:p.Glu116ArgfsTer?
NM_001001431.3:c.345del NP_001001431.1:p.Glu116ArgfsTer?
NM_001001432.3:c.330del NP_001001432.1:p.Glu111ArgfsTer?
NM_001276345.2:c.375del MANE Select NP_001263274.1:p.Glu126ArgfsTer?
NM_001276346.2:c.291+383del NP_001263275.1:n.291+383del
NM_001276347.2:c.345del NP_001263276.1:p.Glu116ArgfsTer?