Linked Data
gnomAD v4:
1-193251840-C-CT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193251843dup , CM000663.2:g.193251843dup | GRCh38 |
| NC_000001.10:g.193220973dup , CM000663.1:g.193220973dup | GRCh37 |
| NC_000001.9:g.191487596dup | NCBI36 |
| NG_012691.1:g.134886dup , LRG_507:g.134886dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367435.5:c.*1131dup MANE Select | ENSP00000356405.4:n.*1131dup | |
| ENST00000635846.1:c.*1131dup | ENSP00000490035.1:n.*1131dup | |
| ENST00000643006.1:c.*1637dup | ENSP00000496633.1:n.*1637dup | |
| ENST00000367435.3:c.*1131dup | ENSP00000356405.3:n.*1131dup | |
| NM_024529.4:c.*1131dup , LRG_507t1:c.*1131dup | NP_078805.3:n.*1131dup | |
| NM_024529.5:c.*1131dup MANE Select | NP_078805.3:n.*1131dup |