Linked Data
ClinVar Variation Id:
202415
dbSNP Id:
rs766840243
ExAC:
2:179428619 G / A
gnomAD v2:
2-179428619-G-A
gnomAD v4:
2-178563892-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178563892G>A , CM000664.2:g.178563892G>A | GRCh38 |
| NC_000002.11:g.179428619G>A , CM000664.1:g.179428619G>A | GRCh37 |
| NC_000002.10:g.179136865G>A | NCBI36 |
| NG_011618.3:g.271911C>T , LRG_391:g.271911C>T | |
| NG_051363.1:g.46066G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.74536C>T (TTN) | ENSP00000343764.6:p.Arg24846Ter | |
| ENST00000342175.11:c.55621C>T (TTN) | ENSP00000340554.6:p.Arg18541Ter | |
| ENST00000359218.10:c.55420C>T (TTN) | ENSP00000352154.5:p.Arg18474Ter | |
| ENST00000342175.10:c.55621C>T (TTN) | ENSP00000340554.6:p.Arg18541Ter | |
| ENST00000342992.10:c.74536C>T (TTN) | ENSP00000343764.6:p.Arg24846Ter | |
| ENST00000359218.9:c.55420C>T (TTN) | ENSP00000352154.5:p.Arg18474Ter | |
| ENST00000460472.6:c.55045C>T (TTN) | ENSP00000434586.1:p.Arg18349Ter | |
| ENST00000589042.5:c.82240C>T (TTN) MANE Select | ENSP00000467141.1:p.Arg27414Ter | |
| ENST00000591111.5:c.77317C>T (TTN) | ENSP00000465570.1:p.Arg25773Ter | |
| ENST00000615779.4:c.77317C>T (TTN) | ENSP00000483597.1:p.Arg25773Ter | |
| NM_001256850.1:c.77317C>T (TTN) | NP_001243779.1:p.Arg25773Ter | |
| NM_001267550.2:c.82240C>T (TTN) MANE Select | NP_001254479.2:p.Arg27414Ter | |
| NM_003319.4:c.55045C>T (TTN) | NP_003310.4:p.Arg18349Ter | |
| NM_133378.4:c.74536C>T (TTN) | NP_596869.4:p.Arg24846Ter | |
| NM_133432.3:c.55420C>T (TTN) | NP_597676.3:p.Arg18474Ter | |
| NM_133437.4:c.55621C>T (TTN) | NP_597681.4:p.Arg18541Ter | |
| NR_038271.1:n.447-7408G>A (TTN-AS1) | ||
| NR_038272.1:n.2044-18680G>A (TTN-AS1) | ||
| XM_011511729.1:c.81337C>T (TTN) | XP_011510031.1:p.Arg27113Ter | |
| XM_011511730.1:c.55231C>T (TTN) | XP_011510032.1:p.Arg18411Ter | |
| XM_011511731.1:c.55090C>T (TTN) | XP_011510033.1:p.Arg18364Ter | |
| XM_017004819.1:c.81133C>T (TTN) | XP_016860308.1:p.Arg27045Ter | |
| XM_017004820.1:c.76531C>T (TTN) | XP_016860309.1:p.Arg25511Ter | |
| XM_017004821.1:c.76528C>T (TTN) | XP_016860310.1:p.Arg25510Ter | |
| XM_017004822.1:c.73570C>T (TTN) | XP_016860311.1:p.Arg24524Ter | |
| XM_017004823.1:c.55186C>T (TTN) | XP_016860312.1:p.Arg18396Ter | |
| XM_024453094.1:c.76681C>T (TTN) | XP_024308862.1:p.Arg25561Ter | |
| XM_024453095.1:c.76678C>T (TTN) | XP_024308863.1:p.Arg25560Ter | |
| XM_024453096.1:c.76111C>T (TTN) | XP_024308864.1:p.Arg25371Ter | |
| XM_024453097.1:c.73453C>T (TTN) | XP_024308865.1:p.Arg24485Ter | |
| XM_024453098.1:c.73372C>T (TTN) | XP_024308866.1:p.Arg24458Ter | |
| XM_024453099.1:c.55135C>T (TTN) | XP_024308867.1:p.Arg18379Ter | |
| XM_024453100.1:c.44989C>T (TTN) | XP_024308868.1:p.Arg14997Ter |