Linked Data
gnomAD v4:
22-20425158-C-CT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.20425159dup , CM000684.2:g.20425159dup | GRCh38 |
| NC_000022.10:g.20779449dup , CM000684.1:g.20779449dup | GRCh37 |
| NC_000022.9:g.19109449dup | NCBI36 |
| NG_031868.2:g.17701dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622235.5:c.*216dup MANE Select | ENSP00000477564.2:n.*216dup | |
| ENST00000615031.4:c.*216dup | ENSP00000479389.1:n.*216dup | |
| ENST00000622235.4:c.*216dup | ENSP00000477564.1:n.*216dup | |
| ENST00000623402.1:c.*216dup | ENSP00000485276.1:n.*216dup | |
| NM_153334.6:c.*216dup | NP_699165.3:n.*216dup | |
| NM_182895.4:c.*216dup | NP_878315.2:n.*216dup | |
| NM_153334.7:c.*216dup | NP_699165.3:n.*216dup | |
| NM_182895.5:c.*216dup MANE Select | NP_878315.2:n.*216dup |