Linked Data
ClinVar Variation Id:
512443
dbSNP Id:
rs780539951
ExAC:
2:179434332 G / A
gnomAD v2:
2-179434332-G-A
gnomAD v3:
2-178569605-G-A
gnomAD v4:
2-178569605-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178569605G>A , CM000664.2:g.178569605G>A | GRCh38 |
| NC_000002.11:g.179434332G>A , CM000664.1:g.179434332G>A | GRCh37 |
| NC_000002.10:g.179142578G>A | NCBI36 |
| NG_011618.3:g.266198C>T , LRG_391:g.266198C>T | |
| NG_051363.1:g.51779G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.68823C>T (TTN) | ENSP00000343764.6:p.Asp22941= | |
| ENST00000342175.11:c.49908C>T (TTN) | ENSP00000340554.6:p.Asp16636= | |
| ENST00000359218.10:c.49707C>T (TTN) | ENSP00000352154.5:p.Asp16569= | |
| ENST00000342175.10:c.49908C>T (TTN) | ENSP00000340554.6:p.Asp16636= | |
| ENST00000342992.10:c.68823C>T (TTN) | ENSP00000343764.6:p.Asp22941= | |
| ENST00000359218.9:c.49707C>T (TTN) | ENSP00000352154.5:p.Asp16569= | |
| ENST00000460472.6:c.49332C>T (TTN) | ENSP00000434586.1:p.Asp16444= | |
| ENST00000589042.5:c.76527C>T (TTN) MANE Select | ENSP00000467141.1:p.Asp25509= | |
| ENST00000591111.5:c.71604C>T (TTN) | ENSP00000465570.1:p.Asp23868= | |
| ENST00000615779.4:c.71604C>T (TTN) | ENSP00000483597.1:p.Asp23868= | |
| NM_001256850.1:c.71604C>T (TTN) | NP_001243779.1:p.Asp23868= | |
| NM_001267550.2:c.76527C>T (TTN) MANE Select | NP_001254479.2:p.Asp25509= | |
| NM_003319.4:c.49332C>T (TTN) | NP_003310.4:p.Asp16444= | |
| NM_133378.4:c.68823C>T (TTN) | NP_596869.4:p.Asp22941= | |
| NM_133432.3:c.49707C>T (TTN) | NP_597676.3:p.Asp16569= | |
| NM_133437.4:c.49908C>T (TTN) | NP_597681.4:p.Asp16636= | |
| NR_038271.1:n.447-1695G>A (TTN-AS1) | ||
| NR_038272.1:n.2044-12967G>A (TTN-AS1) | ||
| XM_011511729.1:c.75624C>T (TTN) | XP_011510031.1:p.Asp25208= | |
| XM_011511730.1:c.49518C>T (TTN) | XP_011510032.1:p.Asp16506= | |
| XM_011511731.1:c.49377C>T (TTN) | XP_011510033.1:p.Asp16459= | |
| XM_017004819.1:c.75420C>T (TTN) | XP_016860308.1:p.Asp25140= | |
| XM_017004820.1:c.70818C>T (TTN) | XP_016860309.1:p.Asp23606= | |
| XM_017004821.1:c.70815C>T (TTN) | XP_016860310.1:p.Asp23605= | |
| XM_017004822.1:c.67857C>T (TTN) | XP_016860311.1:p.Asp22619= | |
| XM_017004823.1:c.49473C>T (TTN) | XP_016860312.1:p.Asp16491= | |
| XM_024453094.1:c.70968C>T (TTN) | XP_024308862.1:p.Asp23656= | |
| XM_024453095.1:c.70965C>T (TTN) | XP_024308863.1:p.Asp23655= | |
| XM_024453096.1:c.70398C>T (TTN) | XP_024308864.1:p.Asp23466= | |
| XM_024453097.1:c.67740C>T (TTN) | XP_024308865.1:p.Asp22580= | |
| XM_024453098.1:c.67659C>T (TTN) | XP_024308866.1:p.Asp22553= | |
| XM_024453099.1:c.49422C>T (TTN) | XP_024308867.1:p.Asp16474= | |
| XM_024453100.1:c.39276C>T (TTN) | XP_024308868.1:p.Asp13092= |