Linked Data
dbSNP Id:
rs1830152342
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134843153_134843157del , CM000671.2:g.134843153_134843157del | GRCh38 |
| NC_000009.11:g.137734999_137735003del , CM000671.1:g.137734999_137735003del | GRCh37 |
| NC_000009.10:g.136874820_136874824del | NCBI36 |
| NG_008030.1:g.206348_206352del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371820.4:c.*850_*854del | ENSP00000360885.4:n.*850_*854del | |
| ENST00000371817.8:c.*850_*854del MANE Select | ENSP00000360882.3:n.*850_*854del | |
| ENST00000371817.7:c.*850_*854del | ENSP00000360882.3:n.*850_*854del | |
| ENST00000618395.4:c.*850_*854del | ENSP00000481360.1:n.*850_*854del | |
| NM_000093.4:c.*850_*854del | NP_000084.3:n.*850_*854del | |
| NM_001278074.1:c.*850_*854del | NP_001265003.1:n.*850_*854del | |
| NR_103451.2:n.71-22948_71-22944del | ||
| NM_000093.5:c.*850_*854del MANE Select | NP_000084.3:n.*850_*854del |