Canonical Allele Identifier: CA004273
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12409
dbSNP Id: rs121964856

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201365297C>T , CM000663.2:g.201365297C>T GRCh38
NC_000001.10:g.201334425C>T , CM000663.1:g.201334425C>T GRCh37
NC_000001.9:g.199601048C>T NCBI36
NG_007556.1:g.17381G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000455702.7:c.290G>A ENSP00000402238.3:p.Arg97Gln
ENST00000367318.10:c.275G>A ENSP00000356287.5:p.Arg92Gln
ENST00000367322.6:c.272G>A ENSP00000356291.2:p.Arg91Gln
ENST00000412633.3:c.275G>A ENSP00000408731.2:p.Arg92Gln
ENST00000422165.6:c.305G>A ENSP00000395163.2:p.Arg102Gln
ENST00000438742.6:c.257G>A ENSP00000414036.2:p.Arg86Gln
ENST00000455702.6:c.290G>A ENSP00000402238.2:p.Arg97Gln
ENST00000651504.1:n.769G>A
ENST00000656932.1:c.305G>A MANE Select ENSP00000499593.1:p.Arg102Gln
ENST00000658476.1:c.275G>A ENSP00000499741.1:p.Arg92Gln
ENST00000660295.1:c.275G>A ENSP00000499418.1:p.Arg92Gln
ENST00000662159.1:c.162+2481G>A ENSP00000499796.1:n.162+2481G>A
ENST00000663843.1:c.*205G>A ENSP00000499590.1:n.*205G>A
ENST00000666449.1:c.275G>A ENSP00000499667.1:p.Arg92Gln
ENST00000236918.11:c.305G>A ENSP00000236918.8:p.Arg102Gln
ENST00000360372.8:c.291+313G>A ENSP00000353535.5:n.291+313G>A
ENST00000367315.6:c.281G>A ENSP00000356284.3:p.Arg94Gln
ENST00000367317.8:c.260G>A ENSP00000356286.5:p.Arg87Gln
ENST00000367318.9:c.275G>A ENSP00000356287.5:p.Arg92Gln
ENST00000367320.6:c.291+313G>A ENSP00000356289.2:n.291+313G>A
ENST00000367322.5:c.275G>A ENSP00000356291.1:p.Arg92Gln
ENST00000412633.2:c.272G>A ENSP00000408731.1:p.Arg91Gln
ENST00000421663.6:c.98G>A ENSP00000404134.3:p.Arg33Gln
ENST00000422165.5:c.290G>A ENSP00000395163.1:p.Arg97Gln
ENST00000438742.5:c.260G>A ENSP00000414036.1:p.Arg87Gln
ENST00000455702.5:c.305G>A ENSP00000402238.1:p.Arg102Gln
ENST00000458432.6:c.98G>A ENSP00000387874.3:p.Arg33Gln
ENST00000466570.5:n.531G>A
ENST00000491504.5:n.1514G>A
ENST00000503459.1:n.144G>A
ENST00000509001.5:c.275G>A ENSP00000422031.1:p.Arg92Gln
ENST00000515042.5:n.201G>A
NM_000364.3:c.305G>A NP_000355.2:p.Arg102Gln
NM_001001430.2:c.275G>A NP_001001430.1:p.Arg92Gln
NM_001001431.2:c.275G>A NP_001001431.1:p.Arg92Gln
NM_001001432.2:c.260G>A NP_001001432.1:p.Arg87Gln
NM_001276345.1:c.305G>A NP_001263274.1:p.Arg102Gln
NM_001276346.1:c.291+313G>A NP_001263275.1:n.291+313G>A
NM_001276347.1:c.275G>A NP_001263276.1:p.Arg92Gln
XM_006711508.2:c.275G>A XP_006711571.1:p.Arg92Gln
XM_006711509.2:c.272G>A XP_006711572.1:p.Arg91Gln
XM_011509938.1:c.305G>A XP_011508240.1:p.Arg102Gln
XM_011509939.1:c.302G>A XP_011508241.1:p.Arg101Gln
XM_011509940.1:c.305G>A XP_011508242.1:p.Arg102Gln
XM_011509941.1:c.302G>A XP_011508243.1:p.Arg101Gln
XM_011509942.1:c.260G>A XP_011508244.1:p.Arg87Gln
XM_011509943.1:c.260G>A XP_011508245.1:p.Arg87Gln
XM_011509944.1:c.257G>A XP_011508246.1:p.Arg86Gln
XM_011509945.1:c.305G>A XP_011508247.1:p.Arg102Gln
XM_011509946.1:c.98G>A XP_011508248.1:p.Arg33Gln
XM_006711508.3:c.275G>A XP_006711571.1:p.Arg92Gln
XM_006711509.3:c.272G>A XP_006711572.1:p.Arg91Gln
XM_011509938.2:c.305G>A XP_011508240.1:p.Arg102Gln
XM_011509940.2:c.305G>A XP_011508242.1:p.Arg102Gln
XM_011509941.2:c.302G>A XP_011508243.1:p.Arg101Gln
XM_011509942.2:c.260G>A XP_011508244.1:p.Arg87Gln
XM_011509943.2:c.260G>A XP_011508245.1:p.Arg87Gln
XM_011509944.2:c.257G>A XP_011508246.1:p.Arg86Gln
XM_017002216.2:c.275G>A XP_016857705.1:p.Arg92Gln
XM_017002217.1:c.275G>A XP_016857706.1:p.Arg92Gln
XM_024449450.1:c.305G>A XP_024305218.1:p.Arg102Gln
XM_024449454.1:c.272G>A XP_024305222.1:p.Arg91Gln
XM_024449455.1:c.275G>A XP_024305223.1:p.Arg92Gln
NM_000364.4:c.305G>A NP_000355.2:p.Arg102Gln
NM_001001430.3:c.275G>A NP_001001430.1:p.Arg92Gln
NM_001001431.3:c.275G>A NP_001001431.1:p.Arg92Gln
NM_001001432.3:c.260G>A NP_001001432.1:p.Arg87Gln
NM_001276345.2:c.305G>A MANE Select NP_001263274.1:p.Arg102Gln
NM_001276346.2:c.291+313G>A NP_001263275.1:n.291+313G>A
NM_001276347.2:c.275G>A NP_001263276.1:p.Arg92Gln