Linked Data
ClinVar Variation Id:
229446
dbSNP Id:
rs772152172
ExAC:
2:179478998 G / A
gnomAD v2:
2-179478998-G-A
gnomAD v3:
2-178614271-G-A
gnomAD v4:
2-178614271-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178614271G>A , CM000664.2:g.178614271G>A | GRCh38 |
| NC_000002.11:g.179478998G>A , CM000664.1:g.179478998G>A | GRCh37 |
| NC_000002.10:g.179187243G>A | NCBI36 |
| NG_011618.3:g.221532C>T , LRG_391:g.221532C>T | |
| NG_051363.1:g.96445G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.41422C>T (TTN) | ENSP00000343764.6:p.Arg13808Cys | |
| ENST00000342175.11:c.22507C>T (TTN) | ENSP00000340554.6:p.Arg7503Cys | |
| ENST00000359218.10:c.22306C>T (TTN) | ENSP00000352154.5:p.Arg7436Cys | |
| ENST00000342175.10:c.22507C>T (TTN) | ENSP00000340554.6:p.Arg7503Cys | |
| ENST00000342992.10:c.41422C>T (TTN) | ENSP00000343764.6:p.Arg13808Cys | |
| ENST00000359218.9:c.22306C>T (TTN) | ENSP00000352154.5:p.Arg7436Cys | |
| ENST00000460472.6:c.21931C>T (TTN) | ENSP00000434586.1:p.Arg7311Cys | |
| ENST00000589042.5:c.49126C>T (TTN) MANE Select | ENSP00000467141.1:p.Arg16376Cys | |
| ENST00000591111.5:c.44203C>T (TTN) | ENSP00000465570.1:p.Arg14735Cys | |
| ENST00000615779.4:c.44203C>T (TTN) | ENSP00000483597.1:p.Arg14735Cys | |
| NM_001256850.1:c.44203C>T (TTN) | NP_001243779.1:p.Arg14735Cys | |
| NM_001267550.2:c.49126C>T (TTN) MANE Select | NP_001254479.2:p.Arg16376Cys | |
| NM_003319.4:c.21931C>T (TTN) | NP_003310.4:p.Arg7311Cys | |
| NM_133378.4:c.41422C>T (TTN) | NP_596869.4:p.Arg13808Cys | |
| NM_133432.3:c.22306C>T (TTN) | NP_597676.3:p.Arg7436Cys | |
| NM_133437.4:c.22507C>T (TTN) | NP_597681.4:p.Arg7503Cys | |
| NR_038271.1:n.1019G>A (TTN-AS1) | ||
| XM_011511729.1:c.48223C>T (TTN) | XP_011510031.1:p.Arg16075Cys | |
| XM_011511730.1:c.22117C>T (TTN) | XP_011510032.1:p.Arg7373Cys | |
| XM_011511731.1:c.21976C>T (TTN) | XP_011510033.1:p.Arg7326Cys | |
| XM_017004819.1:c.48019C>T (TTN) | XP_016860308.1:p.Arg16007Cys | |
| XM_017004820.1:c.43417C>T (TTN) | XP_016860309.1:p.Arg14473Cys | |
| XM_017004821.1:c.43414C>T (TTN) | XP_016860310.1:p.Arg14472Cys | |
| XM_017004822.1:c.40456C>T (TTN) | XP_016860311.1:p.Arg13486Cys | |
| XM_017004823.1:c.22072C>T (TTN) | XP_016860312.1:p.Arg7358Cys | |
| XM_024453094.1:c.43567C>T (TTN) | XP_024308862.1:p.Arg14523Cys | |
| XM_024453095.1:c.43564C>T (TTN) | XP_024308863.1:p.Arg14522Cys | |
| XM_024453096.1:c.42997C>T (TTN) | XP_024308864.1:p.Arg14333Cys | |
| XM_024453097.1:c.40339C>T (TTN) | XP_024308865.1:p.Arg13447Cys | |
| XM_024453098.1:c.40258C>T (TTN) | XP_024308866.1:p.Arg13420Cys | |
| XM_024453099.1:c.22021C>T (TTN) | XP_024308867.1:p.Arg7341Cys | |
| XM_024453100.1:c.11875C>T (TTN) | XP_024308868.1:p.Arg3959Cys |