Linked Data
dbSNP Id:
rs1420778609
gnomAD v2:
2-179479983-T-C
gnomAD v3:
2-178615256-T-C
gnomAD v4:
2-178615256-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178615256T>C , CM000664.2:g.178615256T>C | GRCh38 |
| NC_000002.11:g.179479983T>C , CM000664.1:g.179479983T>C | GRCh37 |
| NC_000002.10:g.179188228T>C | NCBI36 |
| NG_011618.3:g.220547A>G , LRG_391:g.220547A>G | |
| NG_051363.1:g.97430T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.40934+51A>G (TTN) | ENSP00000343764.6:n.40934+51A>G | |
| ENST00000342175.11:c.22019+51A>G (TTN) | ENSP00000340554.6:n.22019+51A>G | |
| ENST00000359218.10:c.21818+51A>G (TTN) | ENSP00000352154.5:n.21818+51A>G | |
| ENST00000342175.10:c.22019+51A>G (TTN) | ENSP00000340554.6:n.22019+51A>G | |
| ENST00000342992.10:c.40934+51A>G (TTN) | ENSP00000343764.6:n.40934+51A>G | |
| ENST00000359218.9:c.21818+51A>G (TTN) | ENSP00000352154.5:n.21818+51A>G | |
| ENST00000460472.6:c.21443+51A>G (TTN) | ENSP00000434586.1:n.21443+51A>G | |
| ENST00000589042.5:c.48638+51A>G (TTN) MANE Select | ENSP00000467141.1:n.48638+51A>G | |
| ENST00000591111.5:c.43715+51A>G (TTN) | ENSP00000465570.1:n.43715+51A>G | |
| ENST00000615779.4:c.43715+51A>G (TTN) | ENSP00000483597.1:n.43715+51A>G | |
| NM_001256850.1:c.43715+51A>G (TTN) | NP_001243779.1:n.43715+51A>G | |
| NM_001267550.2:c.48638+51A>G (TTN) MANE Select | NP_001254479.2:n.48638+51A>G | |
| NM_003319.4:c.21443+51A>G (TTN) | NP_003310.4:n.21443+51A>G | |
| NM_133378.4:c.40934+51A>G (TTN) | NP_596869.4:n.40934+51A>G | |
| NM_133432.3:c.21818+51A>G (TTN) | NP_597676.3:n.21818+51A>G | |
| NM_133437.4:c.22019+51A>G (TTN) | NP_597681.4:n.22019+51A>G | |
| NR_038271.1:n.1553-67T>C (TTN-AS1) | ||
| XM_011511729.1:c.47735+51A>G (TTN) | XP_011510031.1:n.47735+51A>G | |
| XM_011511730.1:c.21629+51A>G (TTN) | XP_011510032.1:n.21629+51A>G | |
| XM_011511731.1:c.21488+51A>G (TTN) | XP_011510033.1:n.21488+51A>G | |
| XM_017004819.1:c.47531+51A>G (TTN) | XP_016860308.1:n.47531+51A>G | |
| XM_017004820.1:c.42929+51A>G (TTN) | XP_016860309.1:n.42929+51A>G | |
| XM_017004821.1:c.42926+51A>G (TTN) | XP_016860310.1:n.42926+51A>G | |
| XM_017004822.1:c.39968+51A>G (TTN) | XP_016860311.1:n.39968+51A>G | |
| XM_017004823.1:c.21584+51A>G (TTN) | XP_016860312.1:n.21584+51A>G | |
| XM_024453094.1:c.43079+51A>G (TTN) | XP_024308862.1:n.43079+51A>G | |
| XM_024453095.1:c.43076+51A>G (TTN) | XP_024308863.1:n.43076+51A>G | |
| XM_024453096.1:c.42509+51A>G (TTN) | XP_024308864.1:n.42509+51A>G | |
| XM_024453097.1:c.39851+51A>G (TTN) | XP_024308865.1:n.39851+51A>G | |
| XM_024453098.1:c.39770+51A>G (TTN) | XP_024308866.1:n.39770+51A>G | |
| XM_024453099.1:c.21533+51A>G (TTN) | XP_024308867.1:n.21533+51A>G | |
| XM_024453100.1:c.11387+51A>G (TTN) | XP_024308868.1:n.11387+51A>G |