Linked Data
gnomAD v4:
15-74755158-CTTCCT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74755162_74755166del , CM000677.2:g.74755162_74755166del | GRCh38 |
| NC_000015.9:g.75047503_75047507del , CM000677.1:g.75047503_75047507del | GRCh37 |
| NC_000015.8:g.72834556_72834560del | NCBI36 |
| NG_008431.1:g.37621_37625del | |
| NG_008431.2:g.37621_37625del | |
| NG_061543.1:g.11318_11322del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.*74_*78del MANE Select | ENSP00000342007.4:n.*74_*78del | |
| ENST00000343932.4:c.*74_*78del | ENSP00000342007.4:n.*74_*78del | |
| NM_000761.4:c.*74_*78del | NP_000752.2:n.*74_*78del | |
| NM_000761.5:c.*74_*78del MANE Select | NP_000752.2:n.*74_*78del |