Canonical Allele Identifier: CA1219711131
Gene: TNNT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201363296C= , CM000663.2:g.201363296C= GRCh38
NC_000001.10:g.201332424C= , CM000663.1:g.201332424C= GRCh37
NC_000001.9:g.199599047C= NCBI36
NG_007556.1:g.19382G=

Transcript Alleles

HGVS Amino-acid change
ENST00000455702.7:c.585G= ENSP00000402238.3:p.Lys195=
ENST00000367318.10:c.570G= ENSP00000356287.5:p.Lys190=
ENST00000367322.6:c.567G= ENSP00000356291.2:p.Lys189=
ENST00000412633.3:c.570G= ENSP00000408731.2:p.Lys190=
ENST00000422165.6:c.600G= ENSP00000395163.2:p.Lys200=
ENST00000438742.6:c.552G= ENSP00000414036.2:p.Lys184=
ENST00000455702.6:c.585G= ENSP00000402238.2:p.Lys195=
ENST00000651504.1:n.1064G=
ENST00000656932.1:c.600G= MANE Select ENSP00000499593.1:p.Lys200=
ENST00000658476.1:c.570G= ENSP00000499741.1:p.Lys190=
ENST00000660295.1:c.570G= ENSP00000499418.1:p.Lys190=
ENST00000662159.1:c.163-1297G= ENSP00000499796.1:n.163-1297G=
ENST00000663843.1:c.*500G= ENSP00000499590.1:n.*500G=
ENST00000666449.1:c.570G= ENSP00000499667.1:p.Lys190=
ENST00000236918.11:c.600G= ENSP00000236918.8:p.Lys200=
ENST00000360372.8:c.480G= ENSP00000353535.5:p.Lys160=
ENST00000367315.6:c.576G= ENSP00000356284.3:p.Lys192=
ENST00000367317.8:c.555G= ENSP00000356286.5:p.Lys185=
ENST00000367318.9:c.570G= ENSP00000356287.5:p.Lys190=
ENST00000367320.6:c.480G= ENSP00000356289.2:p.Lys160=
ENST00000367322.5:c.570G= ENSP00000356291.1:p.Lys190=
ENST00000421663.6:c.393G= ENSP00000404134.3:p.Lys131=
ENST00000438742.5:c.555G= ENSP00000414036.1:p.Lys185=
ENST00000458432.6:c.393G= ENSP00000387874.3:p.Lys131=
ENST00000460780.5:n.893G=
ENST00000476888.5:n.55G=
ENST00000491504.5:n.1809G=
ENST00000509001.5:c.570G= ENSP00000422031.1:p.Lys190=
ENST00000515042.5:n.496G=
NM_000364.3:c.600G= NP_000355.2:p.Lys200=
NM_001001430.2:c.570G= NP_001001430.1:p.Lys190=
NM_001001431.2:c.570G= NP_001001431.1:p.Lys190=
NM_001001432.2:c.555G= NP_001001432.1:p.Lys185=
NM_001276345.1:c.600G= NP_001263274.1:p.Lys200=
NM_001276346.1:c.480G= NP_001263275.1:p.Lys160=
NM_001276347.1:c.570G= NP_001263276.1:p.Lys190=
XM_006711508.2:c.570G= XP_006711571.1:p.Lys190=
XM_006711509.2:c.567G= XP_006711572.1:p.Lys189=
XM_011509938.1:c.600G= XP_011508240.1:p.Lys200=
XM_011509939.1:c.597G= XP_011508241.1:p.Lys199=
XM_011509940.1:c.600G= XP_011508242.1:p.Lys200=
XM_011509941.1:c.597G= XP_011508243.1:p.Lys199=
XM_011509942.1:c.555G= XP_011508244.1:p.Lys185=
XM_011509943.1:c.555G= XP_011508245.1:p.Lys185=
XM_011509944.1:c.552G= XP_011508246.1:p.Lys184=
XM_011509946.1:c.393G= XP_011508248.1:p.Lys131=
XM_006711508.3:c.570G= XP_006711571.1:p.Lys190=
XM_006711509.3:c.567G= XP_006711572.1:p.Lys189=
XM_011509938.2:c.600G= XP_011508240.1:p.Lys200=
XM_011509940.2:c.600G= XP_011508242.1:p.Lys200=
XM_011509941.2:c.597G= XP_011508243.1:p.Lys199=
XM_011509942.2:c.555G= XP_011508244.1:p.Lys185=
XM_011509943.2:c.555G= XP_011508245.1:p.Lys185=
XM_011509944.2:c.552G= XP_011508246.1:p.Lys184=
XM_017002216.2:c.570G= XP_016857705.1:p.Lys190=
XM_017002217.1:c.570G= XP_016857706.1:p.Lys190=
XM_024449450.1:c.600G= XP_024305218.1:p.Lys200=
XM_024449454.1:c.567G= XP_024305222.1:p.Lys189=
XM_024449455.1:c.570G= XP_024305223.1:p.Lys190=
NM_000364.4:c.600G= NP_000355.2:p.Lys200=
NM_001001430.3:c.570G= NP_001001430.1:p.Lys190=
NM_001001431.3:c.570G= NP_001001431.1:p.Lys190=
NM_001001432.3:c.555G= NP_001001432.1:p.Lys185=
NM_001276345.2:c.600G= MANE Select NP_001263274.1:p.Lys200=
NM_001276346.2:c.480G= NP_001263275.1:p.Lys160=
NM_001276347.2:c.570G= NP_001263276.1:p.Lys190=