MyVariant.info:
GRCh37
chr2:g.179451437T>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178586710T>C , CM000664.2:g.178586710T>C | GRCh38 |
| NC_000002.11:g.179451437T>C , CM000664.1:g.179451437T>C | GRCh37 |
| NC_000002.10:g.179159683T>C | NCBI36 |
| NG_011618.3:g.249093A>G , LRG_391:g.249093A>G | |
| NG_051363.1:g.68884T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.56487A>G (TTN) | ENSP00000343764.6:p.Lys18829= | |
| ENST00000342175.11:c.37572A>G (TTN) | ENSP00000340554.6:p.Lys12524= | |
| ENST00000359218.10:c.37371A>G (TTN) | ENSP00000352154.5:p.Lys12457= | |
| ENST00000342175.10:c.37572A>G (TTN) | ENSP00000340554.6:p.Lys12524= | |
| ENST00000342992.10:c.56487A>G (TTN) | ENSP00000343764.6:p.Lys18829= | |
| ENST00000359218.9:c.37371A>G (TTN) | ENSP00000352154.5:p.Lys12457= | |
| ENST00000460472.6:c.36996A>G (TTN) | ENSP00000434586.1:p.Lys12332= | |
| ENST00000589042.5:c.64191A>G (TTN) MANE Select | ENSP00000467141.1:p.Lys21397= | |
| ENST00000591111.5:c.59268A>G (TTN) | ENSP00000465570.1:p.Lys19756= | |
| ENST00000615779.4:c.59268A>G (TTN) | ENSP00000483597.1:p.Lys19756= | |
| NM_001256850.1:c.59268A>G (TTN) | NP_001243779.1:p.Lys19756= | |
| NM_001267550.2:c.64191A>G (TTN) MANE Select | NP_001254479.2:p.Lys21397= | |
| NM_003319.4:c.36996A>G (TTN) | NP_003310.4:p.Lys12332= | |
| NM_133378.4:c.56487A>G (TTN) | NP_596869.4:p.Lys18829= | |
| NM_133432.3:c.37371A>G (TTN) | NP_597676.3:p.Lys12457= | |
| NM_133437.4:c.37572A>G (TTN) | NP_597681.4:p.Lys12524= | |
| NR_038271.1:n.597-10886T>C (TTN-AS1) | ||
| NR_038272.1:n.3188+1717T>C (TTN-AS1) | ||
| XM_011511729.1:c.63288A>G (TTN) | XP_011510031.1:p.Lys21096= | |
| XM_011511730.1:c.37182A>G (TTN) | XP_011510032.1:p.Lys12394= | |
| XM_011511731.1:c.37041A>G (TTN) | XP_011510033.1:p.Lys12347= | |
| XM_017004819.1:c.63084A>G (TTN) | XP_016860308.1:p.Lys21028= | |
| XM_017004820.1:c.58482A>G (TTN) | XP_016860309.1:p.Lys19494= | |
| XM_017004821.1:c.58479A>G (TTN) | XP_016860310.1:p.Lys19493= | |
| XM_017004822.1:c.55521A>G (TTN) | XP_016860311.1:p.Lys18507= | |
| XM_017004823.1:c.37137A>G (TTN) | XP_016860312.1:p.Lys12379= | |
| XM_024453094.1:c.58632A>G (TTN) | XP_024308862.1:p.Lys19544= | |
| XM_024453095.1:c.58629A>G (TTN) | XP_024308863.1:p.Lys19543= | |
| XM_024453096.1:c.58062A>G (TTN) | XP_024308864.1:p.Lys19354= | |
| XM_024453097.1:c.55404A>G (TTN) | XP_024308865.1:p.Lys18468= | |
| XM_024453098.1:c.55323A>G (TTN) | XP_024308866.1:p.Lys18441= | |
| XM_024453099.1:c.37086A>G (TTN) | XP_024308867.1:p.Lys12362= | |
| XM_024453100.1:c.26940A>G (TTN) | XP_024308868.1:p.Lys8980= |