Canonical Allele Identifier: CA1219709385

Gene: TNNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359178_201359179delinsAG , CM000663.2:g.201359178_201359179delinsAG	GRCh38
NC_000001.10:g.201328306_201328307delinsAG , CM000663.1:g.201328306_201328307delinsAG	GRCh37
NC_000001.9:g.199594929_199594930delinsAG	NCBI36
NG_007556.1:g.23499_23500delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.*31_*32delinsCT	ENSP00000402238.3:n.*31_*32delinsCT
ENST00000367318.10:c.*31_*32delinsCT	ENSP00000356287.5:n.*31_*32delinsCT
ENST00000367322.6:c.*31_*32delinsCT	ENSP00000356291.2:n.*31_*32delinsCT
ENST00000412633.3:c.*31_*32delinsCT	ENSP00000408731.2:n.*31_*32delinsCT
ENST00000422165.6:c.*31_*32delinsCT	ENSP00000395163.2:n.*31_*32delinsCT
ENST00000438742.6:c.*31_*32delinsCT	ENSP00000414036.2:n.*31_*32delinsCT
ENST00000651504.1:n.1389_1390delinsCT
ENST00000656932.1:c.*31_*32delinsCT MANE Select	ENSP00000499593.1:n.*31_*32delinsCT
ENST00000658476.1:c.963_964delinsCT	ENSP00000499741.1:p.Ser321=
ENST00000660295.1:c.*31_*32delinsCT	ENSP00000499418.1:n.*31_*32delinsCT
ENST00000662159.1:c.*287_*288delinsCT	ENSP00000499796.1:n.*287_*288delinsCT
ENST00000663843.1:c.*828_*829delinsCT	ENSP00000499590.1:n.*828_*829delinsCT
ENST00000666449.1:c.*173_*174delinsCT	ENSP00000499667.1:n.*173_*174delinsCT
ENST00000236918.11:c.928_929delinsCT	ENSP00000236918.8:n.928_929delinsCT
ENST00000360372.8:c.799_800delinsCT	ENSP00000353535.5:n.799_800delinsCT
ENST00000367315.6:c.*31_*32delinsCT	ENSP00000356284.3:n.*31_*32delinsCT
ENST00000367317.8:c.880_881delinsCT	ENSP00000356286.5:n.880_881delinsCT
ENST00000367318.9:c.*31_*32delinsCT	ENSP00000356287.5:n.*31_*32delinsCT
ENST00000367320.6:c.*31_*32delinsCT	ENSP00000356289.2:n.*31_*32delinsCT
ENST00000367322.5:c.*31_*32delinsCT	ENSP00000356291.1:n.*31_*32delinsCT
ENST00000421663.6:c.*31_*32delinsCT	ENSP00000404134.3:n.*31_*32delinsCT
ENST00000458432.6:c.*31_*32delinsCT	ENSP00000387874.3:n.*31_*32delinsCT
ENST00000460780.5:n.2047_2048delinsCT
ENST00000476888.5:n.345_346delinsCT
ENST00000491504.5:n.2137_2138delinsCT
ENST00000509001.5:c.*31_*32delinsCT	ENSP00000422031.1:n.*31_*32delinsCT
NM_000364.3:c.*31_*32delinsCT	NP_000355.2:n.*31_*32delinsCT
NM_001001430.2:c.*31_*32delinsCT	NP_001001430.1:n.*31_*32delinsCT
NM_001001431.2:c.*31_*32delinsCT	NP_001001431.1:n.*31_*32delinsCT
NM_001001432.2:c.*31_*32delinsCT	NP_001001432.1:n.*31_*32delinsCT
NM_001276345.1:c.*31_*32delinsCT	NP_001263274.1:n.*31_*32delinsCT
NM_001276346.1:c.*31_*32delinsCT	NP_001263275.1:n.*31_*32delinsCT
NM_001276347.1:c.*31_*32delinsCT	NP_001263276.1:n.*31_*32delinsCT
XM_006711508.2:c.*31_*32delinsCT	XP_006711571.1:n.*31_*32delinsCT
XM_006711509.2:c.*31_*32delinsCT	XP_006711572.1:n.*31_*32delinsCT
XM_011509938.1:c.*31_*32delinsCT	XP_011508240.1:n.*31_*32delinsCT
XM_011509939.1:c.*31_*32delinsCT	XP_011508241.1:n.*31_*32delinsCT
XM_011509940.1:c.*31_*32delinsCT	XP_011508242.1:n.*31_*32delinsCT
XM_011509941.1:c.*31_*32delinsCT	XP_011508243.1:n.*31_*32delinsCT
XM_011509942.1:c.*31_*32delinsCT	XP_011508244.1:n.*31_*32delinsCT
XM_011509943.1:c.*31_*32delinsCT	XP_011508245.1:n.*31_*32delinsCT
XM_011509944.1:c.*31_*32delinsCT	XP_011508246.1:n.*31_*32delinsCT
XM_011509946.1:c.*31_*32delinsCT	XP_011508248.1:n.*31_*32delinsCT
XM_006711508.3:c.*31_*32delinsCT	XP_006711571.1:n.*31_*32delinsCT
XM_006711509.3:c.*31_*32delinsCT	XP_006711572.1:n.*31_*32delinsCT
XM_011509938.2:c.*31_*32delinsCT	XP_011508240.1:n.*31_*32delinsCT
XM_011509940.2:c.*31_*32delinsCT	XP_011508242.1:n.*31_*32delinsCT
XM_011509941.2:c.*31_*32delinsCT	XP_011508243.1:n.*31_*32delinsCT
XM_011509942.2:c.*31_*32delinsCT	XP_011508244.1:n.*31_*32delinsCT
XM_011509943.2:c.*31_*32delinsCT	XP_011508245.1:n.*31_*32delinsCT
XM_011509944.2:c.*31_*32delinsCT	XP_011508246.1:n.*31_*32delinsCT
XM_017002216.2:c.*31_*32delinsCT	XP_016857705.1:n.*31_*32delinsCT
XM_017002217.1:c.*31_*32delinsCT	XP_016857706.1:n.*31_*32delinsCT
XM_024449450.1:c.*31_*32delinsCT	XP_024305218.1:n.*31_*32delinsCT
XM_024449454.1:c.*31_*32delinsCT	XP_024305222.1:n.*31_*32delinsCT
XM_024449455.1:c.*31_*32delinsCT	XP_024305223.1:n.*31_*32delinsCT
NM_000364.4:c.*31_*32delinsCT	NP_000355.2:n.*31_*32delinsCT
NM_001001430.3:c.*31_*32delinsCT	NP_001001430.1:n.*31_*32delinsCT
NM_001001431.3:c.*31_*32delinsCT	NP_001001431.1:n.*31_*32delinsCT
NM_001001432.3:c.*31_*32delinsCT	NP_001001432.1:n.*31_*32delinsCT
NM_001276345.2:c.*31_*32delinsCT MANE Select	NP_001263274.1:n.*31_*32delinsCT
NM_001276346.2:c.*31_*32delinsCT	NP_001263275.1:n.*31_*32delinsCT
NM_001276347.2:c.*31_*32delinsCT	NP_001263276.1:n.*31_*32delinsCT