Canonical Allele Identifier: CA1146731115
Gene: TNNT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201365227_201365229delinsTTT , CM000663.2:g.201365227_201365229delinsTTT GRCh38
NC_000001.10:g.201334355_201334357delinsTTT , CM000663.1:g.201334355_201334357delinsTTT GRCh37
NC_000001.9:g.199600978_199600980delinsTTT NCBI36
NG_007556.1:g.17449_17451delinsAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000455702.7:c.358_360delinsAAA ENSP00000402238.3:p.Lys120=
ENST00000367318.10:c.343_345delinsAAA ENSP00000356287.5:p.Lys115=
ENST00000367322.6:c.340_342delinsAAA ENSP00000356291.2:p.Lys114=
ENST00000412633.3:c.343_345delinsAAA ENSP00000408731.2:p.Lys115=
ENST00000422165.6:c.373_375delinsAAA ENSP00000395163.2:p.Lys125=
ENST00000438742.6:c.325_327delinsAAA ENSP00000414036.2:p.Lys109=
ENST00000455702.6:c.358_360delinsAAA ENSP00000402238.2:p.Lys120=
ENST00000651504.1:n.837_839delinsAAA
ENST00000656932.1:c.373_375delinsAAA MANE Select ENSP00000499593.1:p.Lys125=
ENST00000658476.1:c.343_345delinsAAA ENSP00000499741.1:p.Lys115=
ENST00000660295.1:c.343_345delinsAAA ENSP00000499418.1:p.Lys115=
ENST00000662159.1:c.162+2549_162+2551delinsAAA ENSP00000499796.1:n.162+2549_162+2551delinsAAA
ENST00000663843.1:c.*273_*275delinsAAA ENSP00000499590.1:n.*273_*275delinsAAA
ENST00000666449.1:c.343_345delinsAAA ENSP00000499667.1:p.Lys115=
ENST00000236918.11:c.373_375delinsAAA ENSP00000236918.8:p.Lys125=
ENST00000360372.8:c.291+381_291+383delinsAAA ENSP00000353535.5:n.291+381_291+383delinsAAA
ENST00000367315.6:c.349_351delinsAAA ENSP00000356284.3:p.Lys117=
ENST00000367317.8:c.328_330delinsAAA ENSP00000356286.5:p.Lys110=
ENST00000367318.9:c.343_345delinsAAA ENSP00000356287.5:p.Lys115=
ENST00000367320.6:c.291+381_291+383delinsAAA ENSP00000356289.2:n.291+381_291+383delinsAAA
ENST00000367322.5:c.343_345delinsAAA ENSP00000356291.1:p.Lys115=
ENST00000421663.6:c.166_168delinsAAA ENSP00000404134.3:p.Lys56=
ENST00000438742.5:c.328_330delinsAAA ENSP00000414036.1:p.Lys110=
ENST00000455702.5:c.373_375delinsAAA ENSP00000402238.1:p.Lys125=
ENST00000458432.6:c.166_168delinsAAA ENSP00000387874.3:p.Lys56=
ENST00000466570.5:n.599_601delinsAAA
ENST00000491504.5:n.1582_1584delinsAAA
ENST00000503459.1:n.212_214delinsAAA
ENST00000509001.5:c.343_345delinsAAA ENSP00000422031.1:p.Lys115=
ENST00000515042.5:n.269_271delinsAAA
NM_000364.3:c.373_375delinsAAA NP_000355.2:p.Lys125=
NM_001001430.2:c.343_345delinsAAA NP_001001430.1:p.Lys115=
NM_001001431.2:c.343_345delinsAAA NP_001001431.1:p.Lys115=
NM_001001432.2:c.328_330delinsAAA NP_001001432.1:p.Lys110=
NM_001276345.1:c.373_375delinsAAA NP_001263274.1:p.Lys125=
NM_001276346.1:c.291+381_291+383delinsAAA NP_001263275.1:n.291+381_291+383delinsAAA
NM_001276347.1:c.343_345delinsAAA NP_001263276.1:p.Lys115=
XM_006711508.2:c.343_345delinsAAA XP_006711571.1:p.Lys115=
XM_006711509.2:c.340_342delinsAAA XP_006711572.1:p.Lys114=
XM_011509938.1:c.373_375delinsAAA XP_011508240.1:p.Lys125=
XM_011509939.1:c.370_372delinsAAA XP_011508241.1:p.Lys124=
XM_011509940.1:c.373_375delinsAAA XP_011508242.1:p.Lys125=
XM_011509941.1:c.370_372delinsAAA XP_011508243.1:p.Lys124=
XM_011509942.1:c.328_330delinsAAA XP_011508244.1:p.Lys110=
XM_011509943.1:c.328_330delinsAAA XP_011508245.1:p.Lys110=
XM_011509944.1:c.325_327delinsAAA XP_011508246.1:p.Lys109=
XM_011509945.1:c.373_375delinsAAA XP_011508247.1:p.Lys125=
XM_011509946.1:c.166_168delinsAAA XP_011508248.1:p.Lys56=
XM_006711508.3:c.343_345delinsAAA XP_006711571.1:p.Lys115=
XM_006711509.3:c.340_342delinsAAA XP_006711572.1:p.Lys114=
XM_011509938.2:c.373_375delinsAAA XP_011508240.1:p.Lys125=
XM_011509940.2:c.373_375delinsAAA XP_011508242.1:p.Lys125=
XM_011509941.2:c.370_372delinsAAA XP_011508243.1:p.Lys124=
XM_011509942.2:c.328_330delinsAAA XP_011508244.1:p.Lys110=
XM_011509943.2:c.328_330delinsAAA XP_011508245.1:p.Lys110=
XM_011509944.2:c.325_327delinsAAA XP_011508246.1:p.Lys109=
XM_017002216.2:c.343_345delinsAAA XP_016857705.1:p.Lys115=
XM_017002217.1:c.343_345delinsAAA XP_016857706.1:p.Lys115=
XM_024449450.1:c.373_375delinsAAA XP_024305218.1:p.Lys125=
XM_024449454.1:c.340_342delinsAAA XP_024305222.1:p.Lys114=
XM_024449455.1:c.343_345delinsAAA XP_024305223.1:p.Lys115=
NM_000364.4:c.373_375delinsAAA NP_000355.2:p.Lys125=
NM_001001430.3:c.343_345delinsAAA NP_001001430.1:p.Lys115=
NM_001001431.3:c.343_345delinsAAA NP_001001431.1:p.Lys115=
NM_001001432.3:c.328_330delinsAAA NP_001001432.1:p.Lys110=
NM_001276345.2:c.373_375delinsAAA MANE Select NP_001263274.1:p.Lys125=
NM_001276346.2:c.291+381_291+383delinsAAA NP_001263275.1:n.291+381_291+383delinsAAA
NM_001276347.2:c.343_345delinsAAA NP_001263276.1:p.Lys115=