Canonical Allele Identifier: CA089887

Gene: TNNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201364320_201364321insCAGGAACCAGGAAGAGGAG , CM000663.2:g.201364320_201364321insCAGGAACCAGGAAGAGGAG	GRCh38
NC_000001.10:g.201333448_201333449insCAGGAACCAGGAAGAGGAG , CM000663.1:g.201333448_201333449insCAGGAACCAGGAAGAGGAG	GRCh37
NC_000001.9:g.199600071_199600072insCAGGAACCAGGAAGAGGAG	NCBI36
NG_007556.1:g.18357_18358insCTCCTCTTCCTGGTTCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.451_452insCTCCTCTTCCTGGTTCCTG	ENSP00000402238.3:p.Lys151ThrfsTer7
ENST00000367318.10:c.436_437insCTCCTCTTCCTGGTTCCTG	ENSP00000356287.5:p.Lys146ThrfsTer7
ENST00000367322.6:c.433_434insCTCCTCTTCCTGGTTCCTG	ENSP00000356291.2:p.Lys145ThrfsTer7
ENST00000412633.3:c.436_437insCTCCTCTTCCTGGTTCCTG	ENSP00000408731.2:p.Lys146ThrfsTer7
ENST00000422165.6:c.466_467insCTCCTCTTCCTGGTTCCTG	ENSP00000395163.2:p.Lys156ThrfsTer7
ENST00000438742.6:c.418_419insCTCCTCTTCCTGGTTCCTG	ENSP00000414036.2:p.Lys140ThrfsTer7
ENST00000455702.6:c.451_452insCTCCTCTTCCTGGTTCCTG	ENSP00000402238.2:p.Lys151ThrfsTer7
ENST00000651504.1:n.930_931insCTCCTCTTCCTGGTTCCTG
ENST00000656932.1:c.466_467insCTCCTCTTCCTGGTTCCTG MANE Select	ENSP00000499593.1:p.Lys156ThrfsTer7
ENST00000658476.1:c.436_437insCTCCTCTTCCTGGTTCCTG	ENSP00000499741.1:p.Lys146ThrfsTer7
ENST00000660295.1:c.436_437insCTCCTCTTCCTGGTTCCTG	ENSP00000499418.1:p.Lys146ThrfsTer7
ENST00000662159.1:c.163-2322_163-2321insCTCCTCTTCCTGGTTCCTG	ENSP00000499796.1:n.163-2322_163-2321insCTCCTCTTCCTGGTTCCTG
ENST00000663843.1:c.*366_*367insCTCCTCTTCCTGGTTCCTG	ENSP00000499590.1:n.*366_*367insCTCCTCTTCCTGGTTCCTG
ENST00000666449.1:c.436_437insCTCCTCTTCCTGGTTCCTG	ENSP00000499667.1:p.Lys146ThrfsTer7
ENST00000236918.11:c.466_467insCTCCTCTTCCTGGTTCCTG	ENSP00000236918.8:p.Lys156ThrfsTer7
ENST00000360372.8:c.346_347insCTCCTCTTCCTGGTTCCTG	ENSP00000353535.5:p.Lys116ThrfsTer7
ENST00000367315.6:c.442_443insCTCCTCTTCCTGGTTCCTG	ENSP00000356284.3:p.Lys148ThrfsTer7
ENST00000367317.8:c.421_422insCTCCTCTTCCTGGTTCCTG	ENSP00000356286.5:p.Lys141ThrfsTer7
ENST00000367318.9:c.436_437insCTCCTCTTCCTGGTTCCTG	ENSP00000356287.5:p.Lys146ThrfsTer7
ENST00000367320.6:c.346_347insCTCCTCTTCCTGGTTCCTG	ENSP00000356289.2:p.Lys116ThrfsTer7
ENST00000367322.5:c.436_437insCTCCTCTTCCTGGTTCCTG	ENSP00000356291.1:p.Lys146ThrfsTer7
ENST00000421663.6:c.259_260insCTCCTCTTCCTGGTTCCTG	ENSP00000404134.3:p.Lys87ThrfsTer7
ENST00000438742.5:c.421_422insCTCCTCTTCCTGGTTCCTG	ENSP00000414036.1:p.Lys141ThrfsTer7
ENST00000455702.5:c.466_467insCTCCTCTTCCTGGTTCCTG	ENSP00000402238.1:p.Lys156ThrfsTer7
ENST00000458432.6:c.259_260insCTCCTCTTCCTGGTTCCTG	ENSP00000387874.3:p.Lys87ThrfsTer7
ENST00000466570.5:n.692_693insCTCCTCTTCCTGGTTCCTG
ENST00000491504.5:n.1675_1676insCTCCTCTTCCTGGTTCCTG
ENST00000503459.1:n.305_306insCTCCTCTTCCTGGTTCCTG
ENST00000509001.5:c.436_437insCTCCTCTTCCTGGTTCCTG	ENSP00000422031.1:p.Lys146ThrfsTer7
ENST00000515042.5:n.362_363insCTCCTCTTCCTGGTTCCTG
NM_000364.3:c.466_467insCTCCTCTTCCTGGTTCCTG	NP_000355.2:p.Lys156ThrfsTer7
NM_001001430.2:c.436_437insCTCCTCTTCCTGGTTCCTG	NP_001001430.1:p.Lys146ThrfsTer7
NM_001001431.2:c.436_437insCTCCTCTTCCTGGTTCCTG	NP_001001431.1:p.Lys146ThrfsTer7
NM_001001432.2:c.421_422insCTCCTCTTCCTGGTTCCTG	NP_001001432.1:p.Lys141ThrfsTer7
NM_001276345.1:c.466_467insCTCCTCTTCCTGGTTCCTG	NP_001263274.1:p.Lys156ThrfsTer7
NM_001276346.1:c.346_347insCTCCTCTTCCTGGTTCCTG	NP_001263275.1:p.Lys116ThrfsTer7
NM_001276347.1:c.436_437insCTCCTCTTCCTGGTTCCTG	NP_001263276.1:p.Lys146ThrfsTer7
XM_006711508.2:c.436_437insCTCCTCTTCCTGGTTCCTG	XP_006711571.1:p.Lys146ThrfsTer7
XM_006711509.2:c.433_434insCTCCTCTTCCTGGTTCCTG	XP_006711572.1:p.Lys145ThrfsTer7
XM_011509938.1:c.466_467insCTCCTCTTCCTGGTTCCTG	XP_011508240.1:p.Lys156ThrfsTer7
XM_011509939.1:c.463_464insCTCCTCTTCCTGGTTCCTG	XP_011508241.1:p.Lys155ThrfsTer7
XM_011509940.1:c.466_467insCTCCTCTTCCTGGTTCCTG	XP_011508242.1:p.Lys156ThrfsTer7
XM_011509941.1:c.463_464insCTCCTCTTCCTGGTTCCTG	XP_011508243.1:p.Lys155ThrfsTer7
XM_011509942.1:c.421_422insCTCCTCTTCCTGGTTCCTG	XP_011508244.1:p.Lys141ThrfsTer7
XM_011509943.1:c.421_422insCTCCTCTTCCTGGTTCCTG	XP_011508245.1:p.Lys141ThrfsTer7
XM_011509944.1:c.418_419insCTCCTCTTCCTGGTTCCTG	XP_011508246.1:p.Lys140ThrfsTer7
XM_011509945.1:c.466_467insCTCCTCTTCCTGGTTCCTG	XP_011508247.1:p.Lys156ThrfsTer7
XM_011509946.1:c.259_260insCTCCTCTTCCTGGTTCCTG	XP_011508248.1:p.Lys87ThrfsTer7
XM_006711508.3:c.436_437insCTCCTCTTCCTGGTTCCTG	XP_006711571.1:p.Lys146ThrfsTer7
XM_006711509.3:c.433_434insCTCCTCTTCCTGGTTCCTG	XP_006711572.1:p.Lys145ThrfsTer7
XM_011509938.2:c.466_467insCTCCTCTTCCTGGTTCCTG	XP_011508240.1:p.Lys156ThrfsTer7
XM_011509940.2:c.466_467insCTCCTCTTCCTGGTTCCTG	XP_011508242.1:p.Lys156ThrfsTer7
XM_011509941.2:c.463_464insCTCCTCTTCCTGGTTCCTG	XP_011508243.1:p.Lys155ThrfsTer7
XM_011509942.2:c.421_422insCTCCTCTTCCTGGTTCCTG	XP_011508244.1:p.Lys141ThrfsTer7
XM_011509943.2:c.421_422insCTCCTCTTCCTGGTTCCTG	XP_011508245.1:p.Lys141ThrfsTer7
XM_011509944.2:c.418_419insCTCCTCTTCCTGGTTCCTG	XP_011508246.1:p.Lys140ThrfsTer7
XM_017002216.2:c.436_437insCTCCTCTTCCTGGTTCCTG	XP_016857705.1:p.Lys146ThrfsTer7
XM_017002217.1:c.436_437insCTCCTCTTCCTGGTTCCTG	XP_016857706.1:p.Lys146ThrfsTer7
XM_024449450.1:c.466_467insCTCCTCTTCCTGGTTCCTG	XP_024305218.1:p.Lys156ThrfsTer7
XM_024449454.1:c.433_434insCTCCTCTTCCTGGTTCCTG	XP_024305222.1:p.Lys145ThrfsTer7
XM_024449455.1:c.436_437insCTCCTCTTCCTGGTTCCTG	XP_024305223.1:p.Lys146ThrfsTer7
NM_000364.4:c.466_467insCTCCTCTTCCTGGTTCCTG	NP_000355.2:p.Lys156ThrfsTer7
NM_001001430.3:c.436_437insCTCCTCTTCCTGGTTCCTG	NP_001001430.1:p.Lys146ThrfsTer7
NM_001001431.3:c.436_437insCTCCTCTTCCTGGTTCCTG	NP_001001431.1:p.Lys146ThrfsTer7
NM_001001432.3:c.421_422insCTCCTCTTCCTGGTTCCTG	NP_001001432.1:p.Lys141ThrfsTer7
NM_001276345.2:c.466_467insCTCCTCTTCCTGGTTCCTG MANE Select	NP_001263274.1:p.Lys156ThrfsTer7
NM_001276346.2:c.346_347insCTCCTCTTCCTGGTTCCTG	NP_001263275.1:p.Lys116ThrfsTer7
NM_001276347.2:c.436_437insCTCCTCTTCCTGGTTCCTG	NP_001263276.1:p.Lys146ThrfsTer7