Canonical Allele Identifier: CA528093290
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 925600
dbSNP Id: rs1259701355

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201365628_201365629del , CM000663.2:g.201365628_201365629del GRCh38
NC_000001.10:g.201334756_201334757del , CM000663.1:g.201334756_201334757del GRCh37
NC_000001.9:g.199601379_199601380del NCBI36
NG_007556.1:g.17056_17057del

Transcript Alleles

HGVS Amino-acid Change
ENST00000455702.7:c.267_268del ENSP00000402238.3:p.Arg89SerfsTer4
ENST00000367318.10:c.252_253del ENSP00000356287.5:p.Arg84SerfsTer4
ENST00000367322.6:c.249_250del ENSP00000356291.2:p.Arg83SerfsTer4
ENST00000412633.3:c.252_253del ENSP00000408731.2:p.Arg84SerfsTer4
ENST00000422165.6:c.282_283del ENSP00000395163.2:p.Arg94SerfsTer4
ENST00000438742.6:c.234_235del ENSP00000414036.2:p.Arg78SerfsTer4
ENST00000455702.6:c.267_268del ENSP00000402238.2:p.Arg89SerfsTer4
ENST00000651504.1:n.746_747del
ENST00000656932.1:c.282_283del MANE Select ENSP00000499593.1:p.Arg94SerfsTer4
ENST00000658476.1:c.252_253del ENSP00000499741.1:p.Arg84SerfsTer4
ENST00000660295.1:c.252_253del ENSP00000499418.1:p.Arg84SerfsTer4
ENST00000662159.1:c.162+2156_162+2157del ENSP00000499796.1:n.162+2156_162+2157del
ENST00000663843.1:c.*182_*183del ENSP00000499590.1:n.*182_*183del
ENST00000666449.1:c.252_253del ENSP00000499667.1:p.Arg84SerfsTer4
ENST00000236918.11:c.282_283del ENSP00000236918.8:p.Arg94SerfsTer4
ENST00000360372.8:c.279_280del ENSP00000353535.5:p.Arg93SerfsTer4
ENST00000367315.6:c.258_259del ENSP00000356284.3:p.Arg86SerfsTer4
ENST00000367317.8:c.237_238del ENSP00000356286.5:p.Arg79SerfsTer4
ENST00000367318.9:c.252_253del ENSP00000356287.5:p.Arg84SerfsTer4
ENST00000367320.6:c.279_280del ENSP00000356289.2:p.Arg93SerfsTer4
ENST00000367322.5:c.252_253del ENSP00000356291.1:p.Arg84SerfsTer4
ENST00000412633.2:c.249_250del ENSP00000408731.1:p.Arg83SerfsTer4
ENST00000421663.6:c.75_76del ENSP00000404134.3:p.Arg25SerfsTer4
ENST00000422165.5:c.267_268del ENSP00000395163.1:p.Arg89SerfsTer4
ENST00000438742.5:c.237_238del ENSP00000414036.1:p.Arg79SerfsTer4
ENST00000455702.5:c.282_283del ENSP00000402238.1:p.Arg94SerfsTer4
ENST00000458432.6:c.75_76del ENSP00000387874.3:p.Arg25SerfsTer4
ENST00000466570.5:n.508_509del
ENST00000491504.5:n.1491_1492del
ENST00000503459.1:n.121_122del
ENST00000509001.5:c.252_253del ENSP00000422031.1:p.Arg84SerfsTer4
ENST00000515042.5:n.178_179del
NM_000364.3:c.282_283del NP_000355.2:p.Arg94SerfsTer4
NM_001001430.2:c.252_253del NP_001001430.1:p.Arg84SerfsTer4
NM_001001431.2:c.252_253del NP_001001431.1:p.Arg84SerfsTer4
NM_001001432.2:c.237_238del NP_001001432.1:p.Arg79SerfsTer4
NM_001276345.1:c.282_283del NP_001263274.1:p.Arg94SerfsTer4
NM_001276346.1:c.279_280del NP_001263275.1:p.Arg93SerfsTer4
NM_001276347.1:c.252_253del NP_001263276.1:p.Arg84SerfsTer4
XM_006711508.2:c.252_253del XP_006711571.1:p.Arg84SerfsTer4
XM_006711509.2:c.249_250del XP_006711572.1:p.Arg83SerfsTer4
XM_011509938.1:c.282_283del XP_011508240.1:p.Arg94SerfsTer4
XM_011509939.1:c.279_280del XP_011508241.1:p.Arg93SerfsTer4
XM_011509940.1:c.282_283del XP_011508242.1:p.Arg94SerfsTer4
XM_011509941.1:c.279_280del XP_011508243.1:p.Arg93SerfsTer4
XM_011509942.1:c.237_238del XP_011508244.1:p.Arg79SerfsTer4
XM_011509943.1:c.237_238del XP_011508245.1:p.Arg79SerfsTer4
XM_011509944.1:c.234_235del XP_011508246.1:p.Arg78SerfsTer4
XM_011509945.1:c.282_283del XP_011508247.1:p.Arg94SerfsTer4
XM_011509946.1:c.75_76del XP_011508248.1:p.Arg25SerfsTer4
XM_006711508.3:c.252_253del XP_006711571.1:p.Arg84SerfsTer4
XM_006711509.3:c.249_250del XP_006711572.1:p.Arg83SerfsTer4
XM_011509938.2:c.282_283del XP_011508240.1:p.Arg94SerfsTer4
XM_011509940.2:c.282_283del XP_011508242.1:p.Arg94SerfsTer4
XM_011509941.2:c.279_280del XP_011508243.1:p.Arg93SerfsTer4
XM_011509942.2:c.237_238del XP_011508244.1:p.Arg79SerfsTer4
XM_011509943.2:c.237_238del XP_011508245.1:p.Arg79SerfsTer4
XM_011509944.2:c.234_235del XP_011508246.1:p.Arg78SerfsTer4
XM_017002216.2:c.252_253del XP_016857705.1:p.Arg84SerfsTer4
XM_017002217.1:c.252_253del XP_016857706.1:p.Arg84SerfsTer4
XM_024449450.1:c.282_283del XP_024305218.1:p.Arg94SerfsTer4
XM_024449454.1:c.249_250del XP_024305222.1:p.Arg83SerfsTer4
XM_024449455.1:c.252_253del XP_024305223.1:p.Arg84SerfsTer4
NM_000364.4:c.282_283del NP_000355.2:p.Arg94SerfsTer4
NM_001001430.3:c.252_253del NP_001001430.1:p.Arg84SerfsTer4
NM_001001431.3:c.252_253del NP_001001431.1:p.Arg84SerfsTer4
NM_001001432.3:c.237_238del NP_001001432.1:p.Arg79SerfsTer4
NM_001276345.2:c.282_283del MANE Select NP_001263274.1:p.Arg94SerfsTer4
NM_001276346.2:c.279_280del NP_001263275.1:p.Arg93SerfsTer4
NM_001276347.2:c.252_253del NP_001263276.1:p.Arg84SerfsTer4