Linked Data
ClinVar Variation Id:
1563664
dbSNP Id:
rs1440086089
gnomAD v3:
2-178536463-G-A
gnomAD v4:
2-178536463-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178536463G>A , CM000664.2:g.178536463G>A | GRCh38 |
| NC_000002.11:g.179401190G>A , CM000664.1:g.179401190G>A | GRCh37 |
| NC_000002.10:g.179109436G>A | NCBI36 |
| NG_011618.3:g.299340C>T , LRG_391:g.299340C>T | |
| NG_051363.1:g.18637G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.92580C>T (TTN) | ENSP00000343764.6:p.Tyr30860= | |
| ENST00000342175.11:c.73665C>T (TTN) | ENSP00000340554.6:p.Tyr24555= | |
| ENST00000359218.10:c.73464C>T (TTN) | ENSP00000352154.5:p.Tyr24488= | |
| ENST00000342175.10:c.73665C>T (TTN) | ENSP00000340554.6:p.Tyr24555= | |
| ENST00000342992.10:c.92580C>T (TTN) | ENSP00000343764.6:p.Tyr30860= | |
| ENST00000359218.9:c.73464C>T (TTN) | ENSP00000352154.5:p.Tyr24488= | |
| ENST00000460472.6:c.73089C>T (TTN) | ENSP00000434586.1:p.Tyr24363= | |
| ENST00000589042.5:c.100284C>T (TTN) MANE Select | ENSP00000467141.1:p.Tyr33428= | |
| ENST00000591111.5:c.95361C>T (TTN) | ENSP00000465570.1:p.Tyr31787= | |
| ENST00000615779.4:c.95361C>T (TTN) | ENSP00000483597.1:p.Tyr31787= | |
| NM_001256850.1:c.95361C>T (TTN) | NP_001243779.1:p.Tyr31787= | |
| NM_001267550.2:c.100284C>T (TTN) MANE Select | NP_001254479.2:p.Tyr33428= | |
| NM_003319.4:c.73089C>T (TTN) | NP_003310.4:p.Tyr24363= | |
| NM_133378.4:c.92580C>T (TTN) | NP_596869.4:p.Tyr30860= | |
| NM_133432.3:c.73464C>T (TTN) | NP_597676.3:p.Tyr24488= | |
| NM_133437.4:c.73665C>T (TTN) | NP_597681.4:p.Tyr24555= | |
| NR_038271.1:n.446+12827G>A (TTN-AS1) | ||
| NR_038272.1:n.316+635G>A (TTN-AS1) | ||
| XM_011511729.1:c.99381C>T (TTN) | XP_011510031.1:p.Tyr33127= | |
| XM_011511730.1:c.73275C>T (TTN) | XP_011510032.1:p.Tyr24425= | |
| XM_011511731.1:c.73134C>T (TTN) | XP_011510033.1:p.Tyr24378= | |
| XM_017004819.1:c.99177C>T (TTN) | XP_016860308.1:p.Tyr33059= | |
| XM_017004820.1:c.94575C>T (TTN) | XP_016860309.1:p.Tyr31525= | |
| XM_017004821.1:c.94572C>T (TTN) | XP_016860310.1:p.Tyr31524= | |
| XM_017004822.1:c.91614C>T (TTN) | XP_016860311.1:p.Tyr30538= | |
| XM_017004823.1:c.73230C>T (TTN) | XP_016860312.1:p.Tyr24410= | |
| XM_024453094.1:c.94725C>T (TTN) | XP_024308862.1:p.Tyr31575= | |
| XM_024453095.1:c.94722C>T (TTN) | XP_024308863.1:p.Tyr31574= | |
| XM_024453096.1:c.94155C>T (TTN) | XP_024308864.1:p.Tyr31385= | |
| XM_024453097.1:c.91497C>T (TTN) | XP_024308865.1:p.Tyr30499= | |
| XM_024453098.1:c.91416C>T (TTN) | XP_024308866.1:p.Tyr30472= | |
| XM_024453099.1:c.73179C>T (TTN) | XP_024308867.1:p.Tyr24393= | |
| XM_024453100.1:c.63033C>T (TTN) | XP_024308868.1:p.Tyr21011= |