Canonical Allele Identifier: CA1141828506
Gene: TNNT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201361314C= , CM000663.2:g.201361314C= GRCh38
NC_000001.10:g.201330442C= , CM000663.1:g.201330442C= GRCh37
NC_000001.9:g.199597065C= NCBI36
NG_007556.1:g.21364G=

Transcript Alleles

HGVS Amino-acid Change
NM_001276345.2:c.775G= MANE Select NP_001263274.1:p.Asp259=
ENST00000656932.1:c.775G= MANE Select ENSP00000499593.1:p.Asp259=
NM_000364.3:c.766G= NP_000355.2:p.Asp256=
NM_000364.4:c.766G= NP_000355.2:p.Asp256=
NM_001001430.2:c.745G= NP_001001430.1:p.Asp249=
NM_001001430.3:c.745G= NP_001001430.1:p.Asp249=
NM_001001431.2:c.736G= NP_001001431.1:p.Asp246=
NM_001001431.3:c.736G= NP_001001431.1:p.Asp246=
NM_001001432.2:c.727G= NP_001001432.1:p.Asp243=
NM_001001432.3:c.727G= NP_001001432.1:p.Asp243=
NM_001276345.1:c.775G= NP_001263274.1:p.Asp259=
NM_001276346.1:c.646G= NP_001263275.1:p.Asp216=
NM_001276346.2:c.646G= NP_001263275.1:p.Asp216=
NM_001276347.1:c.745G= NP_001263276.1:p.Asp249=
NM_001276347.2:c.745G= NP_001263276.1:p.Asp249=
ENST00000236918.11:c.775G= ENSP00000236918.8:p.Asp259=
ENST00000360372.8:c.646G= ENSP00000353535.5:p.Asp216=
ENST00000367315.6:c.754G= ENSP00000356284.3:p.Asp252=
ENST00000367317.8:c.727G= ENSP00000356286.5:p.Asp243=
ENST00000367318.10:c.745G= ENSP00000356287.5:p.Asp249=
ENST00000367318.9:c.745G= ENSP00000356287.5:p.Asp249=
ENST00000367320.6:c.646G= ENSP00000356289.2:p.Asp216=
ENST00000367322.5:c.736G= ENSP00000356291.1:p.Asp246=
ENST00000367322.6:c.733G= ENSP00000356291.2:p.Asp245=
ENST00000412633.3:c.736G= ENSP00000408731.2:p.Asp246=
ENST00000421663.6:c.559G= ENSP00000404134.3:p.Asp187=
ENST00000422165.6:c.766G= ENSP00000395163.2:p.Asp256=
ENST00000438742.5:c.727G= ENSP00000414036.1:p.Asp243=
ENST00000438742.6:c.724G= ENSP00000414036.2:p.Asp242=
ENST00000455702.6:c.760G= ENSP00000402238.2:p.Asp254=
ENST00000455702.7:c.760G= ENSP00000402238.3:p.Asp254=
ENST00000458432.6:c.559G= ENSP00000387874.3:p.Asp187=
ENST00000460780.5:n.1068G=
ENST00000476888.5:n.192G=
ENST00000477035.1:n.44G=
ENST00000491504.5:n.1984G=
ENST00000509001.5:c.745G= ENSP00000422031.1:p.Asp249=
ENST00000515042.5:n.671G=
ENST00000651504.1:n.1236G=
ENST00000658476.1:c.745G= ENSP00000499741.1:p.Asp249=
ENST00000660295.1:c.745G= ENSP00000499418.1:p.Asp249=
ENST00000662159.1:c.*134G= ENSP00000499796.1:n.*134G=
ENST00000663843.1:c.*675G= ENSP00000499590.1:n.*675G=
ENST00000666449.1:c.*20G= ENSP00000499667.1:n.*20G=
XM_006711508.2:c.745G= XP_006711571.1:p.Asp249=
XM_006711508.3:c.745G= XP_006711571.1:p.Asp249=
XM_006711509.2:c.742G= XP_006711572.1:p.Asp248=
XM_006711509.3:c.742G= XP_006711572.1:p.Asp248=
XM_011509938.1:c.775G= XP_011508240.1:p.Asp259=
XM_011509938.2:c.775G= XP_011508240.1:p.Asp259=
XM_011509939.1:c.772G= XP_011508241.1:p.Asp258=
XM_011509940.1:c.772G= XP_011508242.1:p.Asp258=
XM_011509940.2:c.772G= XP_011508242.1:p.Asp258=
XM_011509941.1:c.769G= XP_011508243.1:p.Asp257=
XM_011509941.2:c.769G= XP_011508243.1:p.Asp257=
XM_011509942.1:c.730G= XP_011508244.1:p.Asp244=
XM_011509942.2:c.730G= XP_011508244.1:p.Asp244=
XM_011509943.1:c.730G= XP_011508245.1:p.Asp244=
XM_011509943.2:c.730G= XP_011508245.1:p.Asp244=
XM_011509944.1:c.727G= XP_011508246.1:p.Asp243=
XM_011509944.2:c.727G= XP_011508246.1:p.Asp243=
XM_011509946.1:c.568G= XP_011508248.1:p.Asp190=
XM_017002216.2:c.742G= XP_016857705.1:p.Asp248=
XM_017002217.1:c.736G= XP_016857706.1:p.Asp246=
XM_024449450.1:c.775G= XP_024305218.1:p.Asp259=
XM_024449454.1:c.742G= XP_024305222.1:p.Asp248=
XM_024449455.1:c.742G= XP_024305223.1:p.Asp248=