Linked Data
ClinVar Variation Id:
466720
dbSNP Id:
rs778021095
ExAC:
2:179397570 C / T
gnomAD v2:
2-179397570-C-T
gnomAD v3:
2-178532843-C-T
gnomAD v4:
2-178532843-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178532843C>T , CM000664.2:g.178532843C>T | GRCh38 |
| NC_000002.11:g.179397570C>T , CM000664.1:g.179397570C>T | GRCh37 |
| NC_000002.10:g.179105816C>T | NCBI36 |
| NG_011618.3:g.302960G>A , LRG_391:g.302960G>A | |
| NG_051363.1:g.15017C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.96068G>A (TTN) | ENSP00000343764.6:p.Arg32023Gln | |
| ENST00000342175.11:c.77153G>A (TTN) | ENSP00000340554.6:p.Arg25718Gln | |
| ENST00000359218.10:c.76952G>A (TTN) | ENSP00000352154.5:p.Arg25651Gln | |
| ENST00000342175.10:c.77153G>A (TTN) | ENSP00000340554.6:p.Arg25718Gln | |
| ENST00000342992.10:c.96068G>A (TTN) | ENSP00000343764.6:p.Arg32023Gln | |
| ENST00000359218.9:c.76952G>A (TTN) | ENSP00000352154.5:p.Arg25651Gln | |
| ENST00000460472.6:c.76577G>A (TTN) | ENSP00000434586.1:p.Arg25526Gln | |
| ENST00000589042.5:c.103772G>A (TTN) MANE Select | ENSP00000467141.1:p.Arg34591Gln | |
| ENST00000591111.5:c.98849G>A (TTN) | ENSP00000465570.1:p.Arg32950Gln | |
| ENST00000615779.4:c.98849G>A (TTN) | ENSP00000483597.1:p.Arg32950Gln | |
| NM_001256850.1:c.98849G>A (TTN) | NP_001243779.1:p.Arg32950Gln | |
| NM_001267550.2:c.103772G>A (TTN) MANE Select | NP_001254479.2:p.Arg34591Gln | |
| NM_003319.4:c.76577G>A (TTN) | NP_003310.4:p.Arg25526Gln | |
| NM_133378.4:c.96068G>A (TTN) | NP_596869.4:p.Arg32023Gln | |
| NM_133432.3:c.76952G>A (TTN) | NP_597676.3:p.Arg25651Gln | |
| NM_133437.4:c.77153G>A (TTN) | NP_597681.4:p.Arg25718Gln | |
| NR_038271.1:n.446+9207C>T (TTN-AS1) | ||
| NR_038272.1:n.220-2889C>T (TTN-AS1) | ||
| XM_011511729.1:c.102869G>A (TTN) | XP_011510031.1:p.Arg34290Gln | |
| XM_011511730.1:c.76763G>A (TTN) | XP_011510032.1:p.Arg25588Gln | |
| XM_011511731.1:c.76622G>A (TTN) | XP_011510033.1:p.Arg25541Gln | |
| XM_017004819.1:c.102665G>A (TTN) | XP_016860308.1:p.Arg34222Gln | |
| XM_017004820.1:c.98063G>A (TTN) | XP_016860309.1:p.Arg32688Gln | |
| XM_017004821.1:c.98060G>A (TTN) | XP_016860310.1:p.Arg32687Gln | |
| XM_017004822.1:c.95102G>A (TTN) | XP_016860311.1:p.Arg31701Gln | |
| XM_017004823.1:c.76718G>A (TTN) | XP_016860312.1:p.Arg25573Gln | |
| XM_024453094.1:c.98213G>A (TTN) | XP_024308862.1:p.Arg32738Gln | |
| XM_024453095.1:c.98210G>A (TTN) | XP_024308863.1:p.Arg32737Gln | |
| XM_024453096.1:c.97643G>A (TTN) | XP_024308864.1:p.Arg32548Gln | |
| XM_024453097.1:c.94985G>A (TTN) | XP_024308865.1:p.Arg31662Gln | |
| XM_024453098.1:c.94904G>A (TTN) | XP_024308866.1:p.Arg31635Gln | |
| XM_024453099.1:c.76667G>A (TTN) | XP_024308867.1:p.Arg25556Gln | |
| XM_024453100.1:c.66521G>A (TTN) | XP_024308868.1:p.Arg22174Gln |