ClinVar RCV:
ClinVar Variation:
dbSNP:
Revel Score:
ENST00000342992
0.261
ENST00000460472
0.261
ENST00000342175
0.261
ENST00000359218
0.261
ENST00000356127
0.261
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178614742T>C , CM000664.2:g.178614742T>C | GRCh38 |
| NC_000002.11:g.179479469T>C , CM000664.1:g.179479469T>C | GRCh37 |
| NC_000002.10:g.179187714T>C | NCBI36 |
| NG_011618.3:g.221061A>G , LRG_391:g.221061A>G | |
| NG_051363.1:g.96916T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.41068A>G (TTN) | ENSP00000343764.6:p.Ile13690Val | |
| ENST00000342175.11:c.22153A>G (TTN) | ENSP00000340554.6:p.Ile7385Val | |
| ENST00000359218.10:c.21952A>G (TTN) | ENSP00000352154.5:p.Ile7318Val | |
| ENST00000342175.10:c.22153A>G (TTN) | ENSP00000340554.6:p.Ile7385Val | |
| ENST00000342992.10:c.41068A>G (TTN) | ENSP00000343764.6:p.Ile13690Val | |
| ENST00000359218.9:c.21952A>G (TTN) | ENSP00000352154.5:p.Ile7318Val | |
| ENST00000460472.6:c.21577A>G (TTN) | ENSP00000434586.1:p.Ile7193Val | |
| ENST00000589042.5:c.48772A>G (TTN) MANE Select | ENSP00000467141.1:p.Ile16258Val | |
| ENST00000591111.5:c.43849A>G (TTN) | ENSP00000465570.1:p.Ile14617Val | |
| ENST00000615779.4:c.43849A>G (TTN) | ENSP00000483597.1:p.Ile14617Val | |
| NM_001256850.1:c.43849A>G (TTN) | NP_001243779.1:p.Ile14617Val | |
| NM_001267550.2:c.48772A>G (TTN) MANE Select | NP_001254479.2:p.Ile16258Val | |
| NM_003319.4:c.21577A>G (TTN) | NP_003310.4:p.Ile7193Val | |
| NM_133378.4:c.41068A>G (TTN) | NP_596869.4:p.Ile13690Val | |
| NM_133432.3:c.21952A>G (TTN) | NP_597676.3:p.Ile7318Val | |
| NM_133437.4:c.22153A>G (TTN) | NP_597681.4:p.Ile7385Val | |
| NR_038271.1:n.1490T>C (TTN-AS1) | ||
| XM_011511729.1:c.47869A>G (TTN) | XP_011510031.1:p.Ile15957Val | |
| XM_011511730.1:c.21763A>G (TTN) | XP_011510032.1:p.Ile7255Val | |
| XM_011511731.1:c.21622A>G (TTN) | XP_011510033.1:p.Ile7208Val | |
| XM_017004819.1:c.47665A>G (TTN) | XP_016860308.1:p.Ile15889Val | |
| XM_017004820.1:c.43063A>G (TTN) | XP_016860309.1:p.Ile14355Val | |
| XM_017004821.1:c.43060A>G (TTN) | XP_016860310.1:p.Ile14354Val | |
| XM_017004822.1:c.40102A>G (TTN) | XP_016860311.1:p.Ile13368Val | |
| XM_017004823.1:c.21718A>G (TTN) | XP_016860312.1:p.Ile7240Val | |
| XM_024453094.1:c.43213A>G (TTN) | XP_024308862.1:p.Ile14405Val | |
| XM_024453095.1:c.43210A>G (TTN) | XP_024308863.1:p.Ile14404Val | |
| XM_024453096.1:c.42643A>G (TTN) | XP_024308864.1:p.Ile14215Val | |
| XM_024453097.1:c.39985A>G (TTN) | XP_024308865.1:p.Ile13329Val | |
| XM_024453098.1:c.39904A>G (TTN) | XP_024308866.1:p.Ile13302Val | |
| XM_024453099.1:c.21667A>G (TTN) | XP_024308867.1:p.Ile7223Val | |
| XM_024453100.1:c.11521A>G (TTN) | XP_024308868.1:p.Ile3841Val |