Linked Data
gnomAD v4:
1-1535348-C-CT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1535348_1535349insT , CM000663.2:g.1535348_1535349insT | GRCh38 |
| NC_000001.10:g.1470728_1470729insT , CM000663.1:g.1470728_1470729insT | GRCh37 |
| NC_000001.9:g.1460591_1460592insT | NCBI36 |
| NG_041807.1:g.10012_10013insA | |
| NG_053035.1:g.28206_28207insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378733.9:c.*10_*11insA MANE Select | ENSP00000368007.4:n.*10_*11insA | |
| ENST00000378733.8:c.*10_*11insA | ENSP00000368007.4:n.*10_*11insA | |
| ENST00000425828.1:c.*10_*11insA | ENSP00000400311.1:n.*10_*11insA | |
| NM_001114748.1:c.*10_*11insA | NP_001108220.1:n.*10_*11insA | |
| NM_001114748.2:c.*10_*11insA MANE Select | NP_001108220.1:n.*10_*11insA |