Canonical Allele Identifier: CA1219711850

Gene: TNNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201365019_201365020delinsGT , CM000663.2:g.201365019_201365020delinsGT	GRCh38
NC_000001.10:g.201334147_201334148delinsGT , CM000663.1:g.201334147_201334148delinsGT	GRCh37
NC_000001.9:g.199600770_199600771delinsGT	NCBI36
NG_007556.1:g.17658_17659delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.396+171_396+172delinsAC	ENSP00000402238.3:n.396+171_396+172delinsAC
ENST00000367318.10:c.381+171_381+172delinsAC	ENSP00000356287.5:n.381+171_381+172delinsAC
ENST00000367322.6:c.378+171_378+172delinsAC	ENSP00000356291.2:n.378+171_378+172delinsAC
ENST00000412633.3:c.381+171_381+172delinsAC	ENSP00000408731.2:n.381+171_381+172delinsAC
ENST00000422165.6:c.411+171_411+172delinsAC	ENSP00000395163.2:n.411+171_411+172delinsAC
ENST00000438742.6:c.363+171_363+172delinsAC	ENSP00000414036.2:n.363+171_363+172delinsAC
ENST00000455702.6:c.396+171_396+172delinsAC	ENSP00000402238.2:n.396+171_396+172delinsAC
ENST00000651504.1:n.875+171_875+172delinsAC
ENST00000656932.1:c.411+171_411+172delinsAC MANE Select	ENSP00000499593.1:n.411+171_411+172delinsAC
ENST00000658476.1:c.381+171_381+172delinsAC	ENSP00000499741.1:n.381+171_381+172delinsAC
ENST00000660295.1:c.381+171_381+172delinsAC	ENSP00000499418.1:n.381+171_381+172delinsAC
ENST00000662159.1:c.162+2758_162+2759delinsAC	ENSP00000499796.1:n.162+2758_162+2759delinsAC
ENST00000663843.1:c.*311+171_*311+172delinsAC	ENSP00000499590.1:n.*311+171_*311+172delinsAC
ENST00000666449.1:c.381+171_381+172delinsAC	ENSP00000499667.1:n.381+171_381+172delinsAC
ENST00000236918.11:c.411+171_411+172delinsAC	ENSP00000236918.8:n.411+171_411+172delinsAC
ENST00000360372.8:c.291+590_291+591delinsAC	ENSP00000353535.5:n.291+590_291+591delinsAC
ENST00000367315.6:c.387+171_387+172delinsAC	ENSP00000356284.3:n.387+171_387+172delinsAC
ENST00000367317.8:c.366+171_366+172delinsAC	ENSP00000356286.5:n.366+171_366+172delinsAC
ENST00000367318.9:c.381+171_381+172delinsAC	ENSP00000356287.5:n.381+171_381+172delinsAC
ENST00000367320.6:c.291+590_291+591delinsAC	ENSP00000356289.2:n.291+590_291+591delinsAC
ENST00000367322.5:c.381+171_381+172delinsAC	ENSP00000356291.1:n.381+171_381+172delinsAC
ENST00000421663.6:c.204+171_204+172delinsAC	ENSP00000404134.3:n.204+171_204+172delinsAC
ENST00000438742.5:c.366+171_366+172delinsAC	ENSP00000414036.1:n.366+171_366+172delinsAC
ENST00000455702.5:c.411+171_411+172delinsAC	ENSP00000402238.1:n.411+171_411+172delinsAC
ENST00000458432.6:c.204+171_204+172delinsAC	ENSP00000387874.3:n.204+171_204+172delinsAC
ENST00000466570.5:n.637+171_637+172delinsAC
ENST00000491504.5:n.1620+171_1620+172delinsAC
ENST00000503459.1:n.250+171_250+172delinsAC
ENST00000509001.5:c.381+171_381+172delinsAC	ENSP00000422031.1:n.381+171_381+172delinsAC
ENST00000515042.5:n.307+171_307+172delinsAC
NM_000364.3:c.411+171_411+172delinsAC	NP_000355.2:n.411+171_411+172delinsAC
NM_001001430.2:c.381+171_381+172delinsAC	NP_001001430.1:n.381+171_381+172delinsAC
NM_001001431.2:c.381+171_381+172delinsAC	NP_001001431.1:n.381+171_381+172delinsAC
NM_001001432.2:c.366+171_366+172delinsAC	NP_001001432.1:n.366+171_366+172delinsAC
NM_001276345.1:c.411+171_411+172delinsAC	NP_001263274.1:n.411+171_411+172delinsAC
NM_001276346.1:c.291+590_291+591delinsAC	NP_001263275.1:n.291+590_291+591delinsAC
NM_001276347.1:c.381+171_381+172delinsAC	NP_001263276.1:n.381+171_381+172delinsAC
XM_006711508.2:c.381+171_381+172delinsAC	XP_006711571.1:n.381+171_381+172delinsAC
XM_006711509.2:c.378+171_378+172delinsAC	XP_006711572.1:n.378+171_378+172delinsAC
XM_011509938.1:c.411+171_411+172delinsAC	XP_011508240.1:n.411+171_411+172delinsAC
XM_011509939.1:c.408+171_408+172delinsAC	XP_011508241.1:n.408+171_408+172delinsAC
XM_011509940.1:c.411+171_411+172delinsAC	XP_011508242.1:n.411+171_411+172delinsAC
XM_011509941.1:c.408+171_408+172delinsAC	XP_011508243.1:n.408+171_408+172delinsAC
XM_011509942.1:c.366+171_366+172delinsAC	XP_011508244.1:n.366+171_366+172delinsAC
XM_011509943.1:c.366+171_366+172delinsAC	XP_011508245.1:n.366+171_366+172delinsAC
XM_011509944.1:c.363+171_363+172delinsAC	XP_011508246.1:n.363+171_363+172delinsAC
XM_011509945.1:c.411+171_411+172delinsAC	XP_011508247.1:n.411+171_411+172delinsAC
XM_011509946.1:c.204+171_204+172delinsAC	XP_011508248.1:n.204+171_204+172delinsAC
XM_006711508.3:c.381+171_381+172delinsAC	XP_006711571.1:n.381+171_381+172delinsAC
XM_006711509.3:c.378+171_378+172delinsAC	XP_006711572.1:n.378+171_378+172delinsAC
XM_011509938.2:c.411+171_411+172delinsAC	XP_011508240.1:n.411+171_411+172delinsAC
XM_011509940.2:c.411+171_411+172delinsAC	XP_011508242.1:n.411+171_411+172delinsAC
XM_011509941.2:c.408+171_408+172delinsAC	XP_011508243.1:n.408+171_408+172delinsAC
XM_011509942.2:c.366+171_366+172delinsAC	XP_011508244.1:n.366+171_366+172delinsAC
XM_011509943.2:c.366+171_366+172delinsAC	XP_011508245.1:n.366+171_366+172delinsAC
XM_011509944.2:c.363+171_363+172delinsAC	XP_011508246.1:n.363+171_363+172delinsAC
XM_017002216.2:c.381+171_381+172delinsAC	XP_016857705.1:n.381+171_381+172delinsAC
XM_017002217.1:c.381+171_381+172delinsAC	XP_016857706.1:n.381+171_381+172delinsAC
XM_024449450.1:c.411+171_411+172delinsAC	XP_024305218.1:n.411+171_411+172delinsAC
XM_024449454.1:c.378+171_378+172delinsAC	XP_024305222.1:n.378+171_378+172delinsAC
XM_024449455.1:c.381+171_381+172delinsAC	XP_024305223.1:n.381+171_381+172delinsAC
NM_000364.4:c.411+171_411+172delinsAC	NP_000355.2:n.411+171_411+172delinsAC
NM_001001430.3:c.381+171_381+172delinsAC	NP_001001430.1:n.381+171_381+172delinsAC
NM_001001431.3:c.381+171_381+172delinsAC	NP_001001431.1:n.381+171_381+172delinsAC
NM_001001432.3:c.366+171_366+172delinsAC	NP_001001432.1:n.366+171_366+172delinsAC
NM_001276345.2:c.411+171_411+172delinsAC MANE Select	NP_001263274.1:n.411+171_411+172delinsAC
NM_001276346.2:c.291+590_291+591delinsAC	NP_001263275.1:n.291+590_291+591delinsAC
NM_001276347.2:c.381+171_381+172delinsAC	NP_001263276.1:n.381+171_381+172delinsAC