Linked Data
gnomAD v4:
6-31269801-CA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31269802del , CM000668.2:g.31269802del | GRCh38 |
| NC_000006.11:g.31237579del , CM000668.1:g.31237579del | GRCh37 |
| NC_000006.10:g.31345558del | NCBI36 |
| NG_029422.2:g.7330del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.1015+164del MANE Select | ENSP00000365402.5:n.1015+164del | |
| ENST00000376228.9:c.1015+164del | ENSP00000365402.5:n.1015+164del | |
| ENST00000376237.8:c.*602+164del | ENSP00000365412.4:n.*602+164del | |
| ENST00000383329.7:c.1015+164del | ENSP00000372819.3:n.1015+164del | |
| ENST00000470363.5:n.497del | ||
| ENST00000487245.5:n.1374+164del | ||
| NM_002117.5:c.1015+164del | NP_002108.4:n.1015+164del | |
| NM_002117.6:c.1015+164del MANE Select | NP_002108.4:n.1015+164del |