Linked Data
ClinVar Variation Id:
165665
dbSNP Id:
rs373085562
ExAC:
2:179401193 G / A
gnomAD v2:
2-179401193-G-A
gnomAD v3:
2-178536466-G-A
gnomAD v4:
2-178536466-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178536466G>A , CM000664.2:g.178536466G>A | GRCh38 |
| NC_000002.11:g.179401193G>A , CM000664.1:g.179401193G>A | GRCh37 |
| NC_000002.10:g.179109439G>A | NCBI36 |
| NG_011618.3:g.299337C>T , LRG_391:g.299337C>T | |
| NG_051363.1:g.18640G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.92577C>T (TTN) | ENSP00000343764.6:p.Tyr30859= | |
| ENST00000342175.11:c.73662C>T (TTN) | ENSP00000340554.6:p.Tyr24554= | |
| ENST00000359218.10:c.73461C>T (TTN) | ENSP00000352154.5:p.Tyr24487= | |
| ENST00000342175.10:c.73662C>T (TTN) | ENSP00000340554.6:p.Tyr24554= | |
| ENST00000342992.10:c.92577C>T (TTN) | ENSP00000343764.6:p.Tyr30859= | |
| ENST00000359218.9:c.73461C>T (TTN) | ENSP00000352154.5:p.Tyr24487= | |
| ENST00000460472.6:c.73086C>T (TTN) | ENSP00000434586.1:p.Tyr24362= | |
| ENST00000589042.5:c.100281C>T (TTN) MANE Select | ENSP00000467141.1:p.Tyr33427= | |
| ENST00000591111.5:c.95358C>T (TTN) | ENSP00000465570.1:p.Tyr31786= | |
| ENST00000615779.4:c.95358C>T (TTN) | ENSP00000483597.1:p.Tyr31786= | |
| NM_001256850.1:c.95358C>T (TTN) | NP_001243779.1:p.Tyr31786= | |
| NM_001267550.2:c.100281C>T (TTN) MANE Select | NP_001254479.2:p.Tyr33427= | |
| NM_003319.4:c.73086C>T (TTN) | NP_003310.4:p.Tyr24362= | |
| NM_133378.4:c.92577C>T (TTN) | NP_596869.4:p.Tyr30859= | |
| NM_133432.3:c.73461C>T (TTN) | NP_597676.3:p.Tyr24487= | |
| NM_133437.4:c.73662C>T (TTN) | NP_597681.4:p.Tyr24554= | |
| NR_038271.1:n.446+12830G>A (TTN-AS1) | ||
| NR_038272.1:n.316+638G>A (TTN-AS1) | ||
| XM_011511729.1:c.99378C>T (TTN) | XP_011510031.1:p.Tyr33126= | |
| XM_011511730.1:c.73272C>T (TTN) | XP_011510032.1:p.Tyr24424= | |
| XM_011511731.1:c.73131C>T (TTN) | XP_011510033.1:p.Tyr24377= | |
| XM_017004819.1:c.99174C>T (TTN) | XP_016860308.1:p.Tyr33058= | |
| XM_017004820.1:c.94572C>T (TTN) | XP_016860309.1:p.Tyr31524= | |
| XM_017004821.1:c.94569C>T (TTN) | XP_016860310.1:p.Tyr31523= | |
| XM_017004822.1:c.91611C>T (TTN) | XP_016860311.1:p.Tyr30537= | |
| XM_017004823.1:c.73227C>T (TTN) | XP_016860312.1:p.Tyr24409= | |
| XM_024453094.1:c.94722C>T (TTN) | XP_024308862.1:p.Tyr31574= | |
| XM_024453095.1:c.94719C>T (TTN) | XP_024308863.1:p.Tyr31573= | |
| XM_024453096.1:c.94152C>T (TTN) | XP_024308864.1:p.Tyr31384= | |
| XM_024453097.1:c.91494C>T (TTN) | XP_024308865.1:p.Tyr30498= | |
| XM_024453098.1:c.91413C>T (TTN) | XP_024308866.1:p.Tyr30471= | |
| XM_024453099.1:c.73176C>T (TTN) | XP_024308867.1:p.Tyr24392= | |
| XM_024453100.1:c.63030C>T (TTN) | XP_024308868.1:p.Tyr21010= |