Linked Data
gnomAD v4:
1-154576262-AG-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154576266del , CM000663.2:g.154576266del | GRCh38 |
| NC_000001.10:g.154548742del , CM000663.1:g.154548742del | GRCh37 |
| NC_000001.9:g.152815366del | NCBI36 |
| NG_008027.1:g.13486del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.*334del MANE Select | ENSP00000357461.3:n.*334del | |
| ENST00000636034.1:c.1505+338del | ENSP00000489703.1:n.1505+338del | |
| ENST00000637900.1:c.*334del | ENSP00000490474.1:n.*334del | |
| ENST00000368476.3:c.*334del | ENSP00000357461.3:n.*334del | |
| NM_000748.2:c.*334del | NP_000739.1:n.*334del | |
| XM_017000180.2:c.*334del | XP_016855669.1:n.*334del | |
| XR_001736952.2:n.2095del | ||
| NM_000748.3:c.*334del MANE Select | NP_000739.1:n.*334del |