Linked Data
gnomAD v4:
17-4734393-T-TA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4734394dup , CM000679.2:g.4734394dup | GRCh38 |
| NC_000017.10:g.4637689dup , CM000679.1:g.4637689dup | GRCh37 |
| NC_000017.9:g.4584438dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293778.12:c.*109dup MANE Select | ENSP00000293778.7:n.*109dup | |
| ENST00000574412.6:c.*212dup | ENSP00000459592.2:n.*212dup | |
| ENST00000293778.10:c.*109dup | ENSP00000293778.6:n.*109dup | |
| ENST00000574412.5:c.*212dup | ENSP00000459592.1:n.*212dup | |
| ENST00000576153.5:n.665dup | ||
| NM_022059.3:c.*109dup | NP_071342.2:n.*109dup | |
| NM_022059.4:c.*109dup | NP_071342.2:n.*109dup | |
| NM_001386809.1:c.*109dup MANE Select | NP_001373738.1:n.*109dup |