Canonical Allele Identifier: CA658656984

Gene: TNNT2

Linked Data

• ClinVar Variation Id: 452747
• ClinVar RCV Id: RCV000646067
• dbSNP Id: rs1553282523

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201365254_201365255delinsAG , CM000663.2:g.201365254_201365255delinsAG	GRCh38
NC_000001.10:g.201334382_201334383delinsAG , CM000663.1:g.201334382_201334383delinsAG	GRCh37
NC_000001.9:g.199601005_199601006delinsAG	NCBI36
NG_007556.1:g.17423_17424delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000455702.7:c.332_333delinsCT	ENSP00000402238.3:p.Ile111Thr
ENST00000367318.10:c.317_318delinsCT	ENSP00000356287.5:p.Ile106Thr
ENST00000367322.6:c.314_315delinsCT	ENSP00000356291.2:p.Ile105Thr
ENST00000412633.3:c.317_318delinsCT	ENSP00000408731.2:p.Ile106Thr
ENST00000422165.6:c.347_348delinsCT	ENSP00000395163.2:p.Ile116Thr
ENST00000438742.6:c.299_300delinsCT	ENSP00000414036.2:p.Ile100Thr
ENST00000455702.6:c.332_333delinsCT	ENSP00000402238.2:p.Ile111Thr
ENST00000651504.1:n.811_812delinsCT
ENST00000656932.1:c.347_348delinsCT MANE Select	ENSP00000499593.1:p.Ile116Thr
ENST00000658476.1:c.317_318delinsCT	ENSP00000499741.1:p.Ile106Thr
ENST00000660295.1:c.317_318delinsCT	ENSP00000499418.1:p.Ile106Thr
ENST00000662159.1:c.162+2523_162+2524delinsCT	ENSP00000499796.1:n.162+2523_162+2524delinsCT
ENST00000663843.1:c.*247_*248delinsCT	ENSP00000499590.1:n.*247_*248delinsCT
ENST00000666449.1:c.317_318delinsCT	ENSP00000499667.1:p.Ile106Thr
ENST00000236918.11:c.347_348delinsCT	ENSP00000236918.8:p.Ile116Thr
ENST00000360372.8:c.291+355_291+356delinsCT	ENSP00000353535.5:n.291+355_291+356delinsCT
ENST00000367315.6:c.323_324delinsCT	ENSP00000356284.3:p.Ile108Thr
ENST00000367317.8:c.302_303delinsCT	ENSP00000356286.5:p.Ile101Thr
ENST00000367318.9:c.317_318delinsCT	ENSP00000356287.5:p.Ile106Thr
ENST00000367320.6:c.291+355_291+356delinsCT	ENSP00000356289.2:n.291+355_291+356delinsCT
ENST00000367322.5:c.317_318delinsCT	ENSP00000356291.1:p.Ile106Thr
ENST00000421663.6:c.140_141delinsCT	ENSP00000404134.3:p.Ile47Thr
ENST00000422165.5:c.332_333delinsCT	ENSP00000395163.1:p.Ile111Thr
ENST00000438742.5:c.302_303delinsCT	ENSP00000414036.1:p.Ile101Thr
ENST00000455702.5:c.347_348delinsCT	ENSP00000402238.1:p.Ile116Thr
ENST00000458432.6:c.140_141delinsCT	ENSP00000387874.3:p.Ile47Thr
ENST00000466570.5:n.573_574delinsCT
ENST00000491504.5:n.1556_1557delinsCT
ENST00000503459.1:n.186_187delinsCT
ENST00000509001.5:c.317_318delinsCT	ENSP00000422031.1:p.Ile106Thr
ENST00000515042.5:n.243_244delinsCT
NM_000364.3:c.347_348delinsCT	NP_000355.2:p.Ile116Thr
NM_001001430.2:c.317_318delinsCT	NP_001001430.1:p.Ile106Thr
NM_001001431.2:c.317_318delinsCT	NP_001001431.1:p.Ile106Thr
NM_001001432.2:c.302_303delinsCT	NP_001001432.1:p.Ile101Thr
NM_001276345.1:c.347_348delinsCT	NP_001263274.1:p.Ile116Thr
NM_001276346.1:c.291+355_291+356delinsCT	NP_001263275.1:n.291+355_291+356delinsCT
NM_001276347.1:c.317_318delinsCT	NP_001263276.1:p.Ile106Thr
XM_006711508.2:c.317_318delinsCT	XP_006711571.1:p.Ile106Thr
XM_006711509.2:c.314_315delinsCT	XP_006711572.1:p.Ile105Thr
XM_011509938.1:c.347_348delinsCT	XP_011508240.1:p.Ile116Thr
XM_011509939.1:c.344_345delinsCT	XP_011508241.1:p.Ile115Thr
XM_011509940.1:c.347_348delinsCT	XP_011508242.1:p.Ile116Thr
XM_011509941.1:c.344_345delinsCT	XP_011508243.1:p.Ile115Thr
XM_011509942.1:c.302_303delinsCT	XP_011508244.1:p.Ile101Thr
XM_011509943.1:c.302_303delinsCT	XP_011508245.1:p.Ile101Thr
XM_011509944.1:c.299_300delinsCT	XP_011508246.1:p.Ile100Thr
XM_011509945.1:c.347_348delinsCT	XP_011508247.1:p.Ile116Thr
XM_011509946.1:c.140_141delinsCT	XP_011508248.1:p.Ile47Thr
XM_006711508.3:c.317_318delinsCT	XP_006711571.1:p.Ile106Thr
XM_006711509.3:c.314_315delinsCT	XP_006711572.1:p.Ile105Thr
XM_011509938.2:c.347_348delinsCT	XP_011508240.1:p.Ile116Thr
XM_011509940.2:c.347_348delinsCT	XP_011508242.1:p.Ile116Thr
XM_011509941.2:c.344_345delinsCT	XP_011508243.1:p.Ile115Thr
XM_011509942.2:c.302_303delinsCT	XP_011508244.1:p.Ile101Thr
XM_011509943.2:c.302_303delinsCT	XP_011508245.1:p.Ile101Thr
XM_011509944.2:c.299_300delinsCT	XP_011508246.1:p.Ile100Thr
XM_017002216.2:c.317_318delinsCT	XP_016857705.1:p.Ile106Thr
XM_017002217.1:c.317_318delinsCT	XP_016857706.1:p.Ile106Thr
XM_024449450.1:c.347_348delinsCT	XP_024305218.1:p.Ile116Thr
XM_024449454.1:c.314_315delinsCT	XP_024305222.1:p.Ile105Thr
XM_024449455.1:c.317_318delinsCT	XP_024305223.1:p.Ile106Thr
NM_000364.4:c.347_348delinsCT	NP_000355.2:p.Ile116Thr
NM_001001430.3:c.317_318delinsCT	NP_001001430.1:p.Ile106Thr
NM_001001431.3:c.317_318delinsCT	NP_001001431.1:p.Ile106Thr
NM_001001432.3:c.302_303delinsCT	NP_001001432.1:p.Ile101Thr
NM_001276345.2:c.347_348delinsCT MANE Select	NP_001263274.1:p.Ile116Thr
NM_001276346.2:c.291+355_291+356delinsCT	NP_001263275.1:n.291+355_291+356delinsCT
NM_001276347.2:c.317_318delinsCT	NP_001263276.1:p.Ile106Thr