Linked Data
ClinVar Variation Id:
191909
dbSNP Id:
rs370890454
ExAC:
2:179441724 C / T
gnomAD v2:
2-179441724-C-T
gnomAD v3:
2-178576997-C-T
gnomAD v4:
2-178576997-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178576997C>T , CM000664.2:g.178576997C>T | GRCh38 |
| NC_000002.11:g.179441724C>T , CM000664.1:g.179441724C>T | GRCh37 |
| NC_000002.10:g.179149970C>T | NCBI36 |
| NG_011618.3:g.258806G>A , LRG_391:g.258806G>A | |
| NG_051363.1:g.59171C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.61634G>A (TTN) | ENSP00000343764.6:p.Arg20545Gln | |
| ENST00000342175.11:c.42719G>A (TTN) | ENSP00000340554.6:p.Arg14240Gln | |
| ENST00000359218.10:c.42518G>A (TTN) | ENSP00000352154.5:p.Arg14173Gln | |
| ENST00000342175.10:c.42719G>A (TTN) | ENSP00000340554.6:p.Arg14240Gln | |
| ENST00000342992.10:c.61634G>A (TTN) | ENSP00000343764.6:p.Arg20545Gln | |
| ENST00000359218.9:c.42518G>A (TTN) | ENSP00000352154.5:p.Arg14173Gln | |
| ENST00000460472.6:c.42143G>A (TTN) | ENSP00000434586.1:p.Arg14048Gln | |
| ENST00000589042.5:c.69338G>A (TTN) MANE Select | ENSP00000467141.1:p.Arg23113Gln | |
| ENST00000591111.5:c.64415G>A (TTN) | ENSP00000465570.1:p.Arg21472Gln | |
| ENST00000615779.4:c.64415G>A (TTN) | ENSP00000483597.1:p.Arg21472Gln | |
| NM_001256850.1:c.64415G>A (TTN) | NP_001243779.1:p.Arg21472Gln | |
| NM_001267550.2:c.69338G>A (TTN) MANE Select | NP_001254479.2:p.Arg23113Gln | |
| NM_003319.4:c.42143G>A (TTN) | NP_003310.4:p.Arg14048Gln | |
| NM_133378.4:c.61634G>A (TTN) | NP_596869.4:p.Arg20545Gln | |
| NM_133432.3:c.42518G>A (TTN) | NP_597676.3:p.Arg14173Gln | |
| NM_133437.4:c.42719G>A (TTN) | NP_597681.4:p.Arg14240Gln | |
| NR_038271.1:n.596+5548C>T (TTN-AS1) | ||
| NR_038272.1:n.2044-5575C>T (TTN-AS1) | ||
| XM_011511729.1:c.68435G>A (TTN) | XP_011510031.1:p.Arg22812Gln | |
| XM_011511730.1:c.42329G>A (TTN) | XP_011510032.1:p.Arg14110Gln | |
| XM_011511731.1:c.42188G>A (TTN) | XP_011510033.1:p.Arg14063Gln | |
| XM_017004819.1:c.68231G>A (TTN) | XP_016860308.1:p.Arg22744Gln | |
| XM_017004820.1:c.63629G>A (TTN) | XP_016860309.1:p.Arg21210Gln | |
| XM_017004821.1:c.63626G>A (TTN) | XP_016860310.1:p.Arg21209Gln | |
| XM_017004822.1:c.60668G>A (TTN) | XP_016860311.1:p.Arg20223Gln | |
| XM_017004823.1:c.42284G>A (TTN) | XP_016860312.1:p.Arg14095Gln | |
| XM_024453094.1:c.63779G>A (TTN) | XP_024308862.1:p.Arg21260Gln | |
| XM_024453095.1:c.63776G>A (TTN) | XP_024308863.1:p.Arg21259Gln | |
| XM_024453096.1:c.63209G>A (TTN) | XP_024308864.1:p.Arg21070Gln | |
| XM_024453097.1:c.60551G>A (TTN) | XP_024308865.1:p.Arg20184Gln | |
| XM_024453098.1:c.60470G>A (TTN) | XP_024308866.1:p.Arg20157Gln | |
| XM_024453099.1:c.42233G>A (TTN) | XP_024308867.1:p.Arg14078Gln | |
| XM_024453100.1:c.32087G>A (TTN) | XP_024308868.1:p.Arg10696Gln |