Canonical Allele Identifier: CA344202311
Gene: TNNT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201359623A>G , CM000663.2:g.201359623A>G GRCh38
NC_000001.10:g.201328751A>G , CM000663.1:g.201328751A>G GRCh37
NC_000001.9:g.199595374A>G NCBI36
NG_007556.1:g.23055T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001276345.2:c.851T>C MANE Select NP_001263274.1:p.Val284Ala
ENST00000656932.1:c.851T>C MANE Select ENSP00000499593.1:p.Val284Ala
NM_000364.3:c.842T>C NP_000355.2:p.Val281Ala
NM_000364.4:c.842T>C NP_000355.2:p.Val281Ala
NM_001001430.2:c.821T>C NP_001001430.1:p.Val274Ala
NM_001001430.3:c.821T>C NP_001001430.1:p.Val274Ala
NM_001001431.2:c.812T>C NP_001001431.1:p.Val271Ala
NM_001001431.3:c.812T>C NP_001001431.1:p.Val271Ala
NM_001001432.2:c.803T>C NP_001001432.1:p.Val268Ala
NM_001001432.3:c.803T>C NP_001001432.1:p.Val268Ala
NM_001276345.1:c.851T>C NP_001263274.1:p.Val284Ala
NM_001276346.1:c.722T>C NP_001263275.1:p.Val241Ala
NM_001276346.2:c.722T>C NP_001263275.1:p.Val241Ala
NM_001276347.1:c.821T>C NP_001263276.1:p.Val274Ala
NM_001276347.2:c.821T>C NP_001263276.1:p.Val274Ala
ENST00000236918.11:c.851T>C ENSP00000236918.8:p.Val284Ala
ENST00000360372.8:c.722T>C ENSP00000353535.5:p.Val241Ala
ENST00000367315.6:c.830T>C ENSP00000356284.3:p.Val277Ala
ENST00000367317.8:c.803T>C ENSP00000356286.5:p.Val268Ala
ENST00000367318.10:c.821T>C ENSP00000356287.5:p.Val274Ala
ENST00000367318.9:c.821T>C ENSP00000356287.5:p.Val274Ala
ENST00000367320.6:c.722T>C ENSP00000356289.2:p.Val241Ala
ENST00000367322.5:c.812T>C ENSP00000356291.1:p.Val271Ala
ENST00000367322.6:c.809T>C ENSP00000356291.2:p.Val270Ala
ENST00000412633.3:c.812T>C ENSP00000408731.2:p.Val271Ala
ENST00000421663.6:c.635T>C ENSP00000404134.3:p.Val212Ala
ENST00000422165.6:c.842T>C ENSP00000395163.2:p.Val281Ala
ENST00000438742.5:c.803T>C ENSP00000414036.1:p.Val268Ala
ENST00000438742.6:c.800T>C ENSP00000414036.2:p.Val267Ala
ENST00000455702.7:c.836T>C ENSP00000402238.3:p.Val279Ala
ENST00000458432.6:c.635T>C ENSP00000387874.3:p.Val212Ala
ENST00000460780.5:n.1970T>C
ENST00000476888.5:n.268T>C
ENST00000491504.5:n.2060T>C
ENST00000509001.5:c.821T>C ENSP00000422031.1:p.Val274Ala
ENST00000651504.1:n.1312T>C
ENST00000658476.1:c.886T>C ENSP00000499741.1:p.Ser296Pro
ENST00000660295.1:c.821T>C ENSP00000499418.1:p.Val274Ala
ENST00000662159.1:c.*210T>C ENSP00000499796.1:n.*210T>C
ENST00000663843.1:c.*751T>C ENSP00000499590.1:n.*751T>C
ENST00000666449.1:c.*96T>C ENSP00000499667.1:n.*96T>C
XM_006711508.2:c.821T>C XP_006711571.1:p.Val274Ala
XM_006711508.3:c.821T>C XP_006711571.1:p.Val274Ala
XM_006711509.2:c.818T>C XP_006711572.1:p.Val273Ala
XM_006711509.3:c.818T>C XP_006711572.1:p.Val273Ala
XM_011509938.1:c.851T>C XP_011508240.1:p.Val284Ala
XM_011509938.2:c.851T>C XP_011508240.1:p.Val284Ala
XM_011509939.1:c.848T>C XP_011508241.1:p.Val283Ala
XM_011509940.1:c.848T>C XP_011508242.1:p.Val283Ala
XM_011509940.2:c.848T>C XP_011508242.1:p.Val283Ala
XM_011509941.1:c.845T>C XP_011508243.1:p.Val282Ala
XM_011509941.2:c.845T>C XP_011508243.1:p.Val282Ala
XM_011509942.1:c.806T>C XP_011508244.1:p.Val269Ala
XM_011509942.2:c.806T>C XP_011508244.1:p.Val269Ala
XM_011509943.1:c.806T>C XP_011508245.1:p.Val269Ala
XM_011509943.2:c.806T>C XP_011508245.1:p.Val269Ala
XM_011509944.1:c.803T>C XP_011508246.1:p.Val268Ala
XM_011509944.2:c.803T>C XP_011508246.1:p.Val268Ala
XM_011509946.1:c.644T>C XP_011508248.1:p.Val215Ala
XM_017002216.2:c.818T>C XP_016857705.1:p.Val273Ala
XM_017002217.1:c.812T>C XP_016857706.1:p.Val271Ala
XM_024449450.1:c.851T>C XP_024305218.1:p.Val284Ala
XM_024449454.1:c.818T>C XP_024305222.1:p.Val273Ala
XM_024449455.1:c.818T>C XP_024305223.1:p.Val273Ala