MyVariant.info:
GRCh37
chr2:g.179451338G>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178586611G>C , CM000664.2:g.178586611G>C | GRCh38 |
| NC_000002.11:g.179451338G>C , CM000664.1:g.179451338G>C | GRCh37 |
| NC_000002.10:g.179159584G>C | NCBI36 |
| NG_011618.3:g.249192C>G , LRG_391:g.249192C>G | |
| NG_051363.1:g.68785G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.56586C>G (TTN) | ENSP00000343764.6:p.Gly18862= | |
| ENST00000342175.11:c.37671C>G (TTN) | ENSP00000340554.6:p.Gly12557= | |
| ENST00000359218.10:c.37470C>G (TTN) | ENSP00000352154.5:p.Gly12490= | |
| ENST00000342175.10:c.37671C>G (TTN) | ENSP00000340554.6:p.Gly12557= | |
| ENST00000342992.10:c.56586C>G (TTN) | ENSP00000343764.6:p.Gly18862= | |
| ENST00000359218.9:c.37470C>G (TTN) | ENSP00000352154.5:p.Gly12490= | |
| ENST00000460472.6:c.37095C>G (TTN) | ENSP00000434586.1:p.Gly12365= | |
| ENST00000589042.5:c.64290C>G (TTN) MANE Select | ENSP00000467141.1:p.Gly21430= | |
| ENST00000591111.5:c.59367C>G (TTN) | ENSP00000465570.1:p.Gly19789= | |
| ENST00000615779.4:c.59367C>G (TTN) | ENSP00000483597.1:p.Gly19789= | |
| NM_001256850.1:c.59367C>G (TTN) | NP_001243779.1:p.Gly19789= | |
| NM_001267550.2:c.64290C>G (TTN) MANE Select | NP_001254479.2:p.Gly21430= | |
| NM_003319.4:c.37095C>G (TTN) | NP_003310.4:p.Gly12365= | |
| NM_133378.4:c.56586C>G (TTN) | NP_596869.4:p.Gly18862= | |
| NM_133432.3:c.37470C>G (TTN) | NP_597676.3:p.Gly12490= | |
| NM_133437.4:c.37671C>G (TTN) | NP_597681.4:p.Gly12557= | |
| NR_038271.1:n.597-10985G>C (TTN-AS1) | ||
| NR_038272.1:n.3188+1618G>C (TTN-AS1) | ||
| XM_011511729.1:c.63387C>G (TTN) | XP_011510031.1:p.Gly21129= | |
| XM_011511730.1:c.37281C>G (TTN) | XP_011510032.1:p.Gly12427= | |
| XM_011511731.1:c.37140C>G (TTN) | XP_011510033.1:p.Gly12380= | |
| XM_017004819.1:c.63183C>G (TTN) | XP_016860308.1:p.Gly21061= | |
| XM_017004820.1:c.58581C>G (TTN) | XP_016860309.1:p.Gly19527= | |
| XM_017004821.1:c.58578C>G (TTN) | XP_016860310.1:p.Gly19526= | |
| XM_017004822.1:c.55620C>G (TTN) | XP_016860311.1:p.Gly18540= | |
| XM_017004823.1:c.37236C>G (TTN) | XP_016860312.1:p.Gly12412= | |
| XM_024453094.1:c.58731C>G (TTN) | XP_024308862.1:p.Gly19577= | |
| XM_024453095.1:c.58728C>G (TTN) | XP_024308863.1:p.Gly19576= | |
| XM_024453096.1:c.58161C>G (TTN) | XP_024308864.1:p.Gly19387= | |
| XM_024453097.1:c.55503C>G (TTN) | XP_024308865.1:p.Gly18501= | |
| XM_024453098.1:c.55422C>G (TTN) | XP_024308866.1:p.Gly18474= | |
| XM_024453099.1:c.37185C>G (TTN) | XP_024308867.1:p.Gly12395= | |
| XM_024453100.1:c.27039C>G (TTN) | XP_024308868.1:p.Gly9013= |