Linked Data
gnomAD v4:
21-45990482-AGGGACGGAGT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45990485_45990494del , CM000683.2:g.45990485_45990494del | GRCh38 |
| NC_000021.8:g.47410399_47410408del , CM000683.1:g.47410399_47410408del | GRCh37 |
| NC_000021.7:g.46234827_46234836del | NCBI36 |
| NG_008674.1:g.13737_13746del , LRG_475:g.13737_13746del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361866.8:c.1002+63_1002+72del MANE Select | ENSP00000355180.3:n.1002+63_1002+72del | |
| ENST00000361866.7:c.1002+63_1002+72del | ENSP00000355180.3:n.1002+63_1002+72del | |
| ENST00000612273.1:c.1002+63_1002+72del | ENSP00000483630.1:n.1002+63_1002+72del | |
| NM_001848.2:c.1002+63_1002+72del , LRG_475t1:c.1002+63_1002+72del | NP_001839.2:n.1002+63_1002+72del | |
| NM_001848.3:c.1002+63_1002+72del MANE Select | NP_001839.2:n.1002+63_1002+72del |