Linked Data
dbSNP Id:
rs71356643
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584050_41584069delinsTTTTTT , CM000679.2:g.41584050_41584069delinsTTTTTT | GRCh38 |
| NC_000017.10:g.39740302_39740321delinsTTTTTT , CM000679.1:g.39740302_39740321delinsTTTTTT | GRCh37 |
| NC_000017.9:g.36993828_36993847delinsTTTTTT | NCBI36 |
| NG_008624.1:g.7827_7846delinsAAAAAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-148_766-129delinsAAAAAA MANE Select | ENSP00000167586.6:n.766-148_766-129delinsAAAAAA | |
| ENST00000167586.6:c.766-148_766-129delinsAAAAAA | ENSP00000167586.6:n.766-148_766-129delinsAAAAAA | |
| ENST00000476662.1:n.216-148_216-129delinsAAAAAA | ||
| NM_000526.4:c.766-148_766-129delinsAAAAAA | NP_000517.2:n.766-148_766-129delinsAAAAAA | |
| NM_000526.5:c.766-148_766-129delinsAAAAAA MANE Select | NP_000517.3:n.766-148_766-129delinsAAAAAA |