Linked Data
ClinVar Variation Id:
487631
ClinVar RCV Id:
RCV000656211
RCV001508034
RCV002358636
RCV002529034
RCV003451293
RCV003451294
RCV003451295
RCV004001215
dbSNP Id:
rs1289914935
gnomAD v2:
1-201342380-C-T
gnomAD v4:
1-201373252-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.201373252C>T , CM000663.2:g.201373252C>T | GRCh38 |
| NC_000001.10:g.201342380C>T , CM000663.1:g.201342380C>T | GRCh37 |
| NC_000001.9:g.199609003C>T | NCBI36 |
| NG_007556.1:g.9426G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000455702.7:c.3G>A (TNNT2) | ENSP00000402238.3:p.Met1Ile | |
| ENST00000367318.10:c.3G>A (TNNT2) | ENSP00000356287.5:p.Met1Ile | |
| ENST00000367322.6:c.3G>A (TNNT2) | ENSP00000356291.2:p.Met1Ile | |
| ENST00000412633.3:c.3G>A (TNNT2) | ENSP00000408731.2:p.Met1Ile | |
| ENST00000422165.6:c.3G>A (TNNT2) | ENSP00000395163.2:p.Met1Ile | |
| ENST00000438742.6:c.3G>A (TNNT2) | ENSP00000414036.2:p.Met1Ile | |
| ENST00000455702.6:c.3G>A (TNNT2) | ENSP00000402238.2:p.Met1Ile | |
| ENST00000656932.1:c.3G>A (TNNT2) MANE Select | ENSP00000499593.1:p.Met1Ile | |
| ENST00000658476.1:c.3G>A (TNNT2) | ENSP00000499741.1:p.Met1Ile | |
| ENST00000660295.1:c.3G>A (TNNT2) | ENSP00000499418.1:p.Met1Ile | |
| ENST00000662159.1:c.3G>A (TNNT2) | ENSP00000499796.1:p.Met1Ile | |
| ENST00000663843.1:c.3G>A (TNNT2) | ENSP00000499590.1:p.Met1Ile | |
| ENST00000666449.1:c.3G>A (TNNT2) | ENSP00000499667.1:p.Met1Ile | |
| ENST00000236918.11:c.3G>A (TNNT2) | ENSP00000236918.8:p.Met1Ile | |
| ENST00000360372.8:c.3G>A (TNNT2) | ENSP00000353535.5:p.Met1Ile | |
| ENST00000367315.6:c.3G>A (TNNT2) | ENSP00000356284.3:p.Met1Ile | |
| ENST00000367317.8:c.3G>A (TNNT2) | ENSP00000356286.5:p.Met1Ile | |
| ENST00000367318.9:c.3G>A (TNNT2) | ENSP00000356287.5:p.Met1Ile | |
| ENST00000367320.6:c.3G>A (TNNT2) | ENSP00000356289.2:p.Met1Ile | |
| ENST00000367322.5:c.3G>A (TNNT2) | ENSP00000356291.1:p.Met1Ile | |
| ENST00000412633.2:c.3G>A (TNNT2) | ENSP00000408731.1:p.Met1Ile | |
| ENST00000421663.6:c.-154G>A (TNNT2) | ENSP00000404134.3:n.-154G>A | |
| ENST00000422165.5:c.3G>A (TNNT2) | ENSP00000395163.1:p.Met1Ile | |
| ENST00000438742.5:c.3G>A (TNNT2) | ENSP00000414036.1:p.Met1Ile | |
| ENST00000455702.5:c.3G>A (TNNT2) | ENSP00000402238.1:p.Met1Ile | |
| ENST00000458432.6:c.-206G>A (TNNT2) | ENSP00000387874.3:n.-206G>A | |
| ENST00000466570.5:n.64G>A (TNNT2) | ||
| ENST00000472177.2:n.75G>A (TNNT2) | ||
| ENST00000475686.5:n.14G>A (TNNT2) | ||
| ENST00000491504.5:n.75G>A (TNNT2) | ||
| ENST00000494095.5:n.2117G>A (TNNT2) | ||
| ENST00000503578.5:c.574G>A (LAD1) | ENSP00000422687.1:p.Val192Ile | |
| ENST00000509001.5:c.3G>A (TNNT2) | ENSP00000422031.1:p.Met1Ile | |
| NM_000364.3:c.3G>A (TNNT2) | NP_000355.2:p.Met1Ile | |
| NM_001001430.2:c.3G>A (TNNT2) | NP_001001430.1:p.Met1Ile | |
| NM_001001431.2:c.3G>A (TNNT2) | NP_001001431.1:p.Met1Ile | |
| NM_001001432.2:c.3G>A (TNNT2) | NP_001001432.1:p.Met1Ile | |
| NM_001276345.1:c.3G>A (TNNT2) | NP_001263274.1:p.Met1Ile | |
| NM_001276346.1:c.3G>A (TNNT2) | NP_001263275.1:p.Met1Ile | |
| NM_001276347.1:c.3G>A (TNNT2) | NP_001263276.1:p.Met1Ile | |
| XM_006711508.2:c.3G>A (TNNT2) | XP_006711571.1:p.Met1Ile | |
| XM_006711509.2:c.3G>A (TNNT2) | XP_006711572.1:p.Met1Ile | |
| XM_011509938.1:c.3G>A (TNNT2) | XP_011508240.1:p.Met1Ile | |
| XM_011509939.1:c.3G>A (TNNT2) | XP_011508241.1:p.Met1Ile | |
| XM_011509940.1:c.3G>A (TNNT2) | XP_011508242.1:p.Met1Ile | |
| XM_011509941.1:c.3G>A (TNNT2) | XP_011508243.1:p.Met1Ile | |
| XM_011509942.1:c.3G>A (TNNT2) | XP_011508244.1:p.Met1Ile | |
| XM_011509943.1:c.3G>A (TNNT2) | XP_011508245.1:p.Met1Ile | |
| XM_011509944.1:c.3G>A (TNNT2) | XP_011508246.1:p.Met1Ile | |
| XM_011509945.1:c.3G>A (TNNT2) | XP_011508247.1:p.Met1Ile | |
| XM_011509946.1:c.-270G>A (TNNT2) | XP_011508248.1:n.-270G>A | |
| XM_006711508.3:c.3G>A (TNNT2) | XP_006711571.1:p.Met1Ile | |
| XM_006711509.3:c.3G>A (TNNT2) | XP_006711572.1:p.Met1Ile | |
| XM_011509938.2:c.3G>A (TNNT2) | XP_011508240.1:p.Met1Ile | |
| XM_011509940.2:c.3G>A (TNNT2) | XP_011508242.1:p.Met1Ile | |
| XM_011509941.2:c.3G>A (TNNT2) | XP_011508243.1:p.Met1Ile | |
| XM_011509942.2:c.3G>A (TNNT2) | XP_011508244.1:p.Met1Ile | |
| XM_011509943.2:c.3G>A (TNNT2) | XP_011508245.1:p.Met1Ile | |
| XM_011509944.2:c.3G>A (TNNT2) | XP_011508246.1:p.Met1Ile | |
| XM_017002216.2:c.3G>A (TNNT2) | XP_016857705.1:p.Met1Ile | |
| XM_017002217.1:c.3G>A (TNNT2) | XP_016857706.1:p.Met1Ile | |
| XM_024449450.1:c.3G>A (TNNT2) | XP_024305218.1:p.Met1Ile | |
| XM_024449454.1:c.3G>A (TNNT2) | XP_024305222.1:p.Met1Ile | |
| XM_024449455.1:c.3G>A (TNNT2) | XP_024305223.1:p.Met1Ile | |
| NM_000364.4:c.3G>A (TNNT2) | NP_000355.2:p.Met1Ile | |
| NM_001001430.3:c.3G>A (TNNT2) | NP_001001430.1:p.Met1Ile | |
| NM_001001431.3:c.3G>A (TNNT2) | NP_001001431.1:p.Met1Ile | |
| NM_001001432.3:c.3G>A (TNNT2) | NP_001001432.1:p.Met1Ile | |
| NM_001276345.2:c.3G>A (TNNT2) MANE Select | NP_001263274.1:p.Met1Ile | |
| NM_001276346.2:c.3G>A (TNNT2) | NP_001263275.1:p.Met1Ile | |
| NM_001276347.2:c.3G>A (TNNT2) | NP_001263276.1:p.Met1Ile |