Linked Data
gnomAD v4:
4-67754364-G-GTTT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67754365_67754366insTTT , CM000666.2:g.67754365_67754366insTTT | GRCh38 |
| NC_000004.11:g.68620083_68620084insTTT , CM000666.1:g.68620083_68620084insTTT | GRCh37 |
| NC_000004.10:g.68302678_68302679insTTT | NCBI36 |
| NG_009293.1:g.6722_6723insAAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226413.5:c.-30_-29insAAA MANE Select | ENSP00000226413.5:n.-30_-29insAAA | |
| NM_000406.2:c.-30_-29insAAA | NP_000397.1:n.-30_-29insAAA | |
| NM_001012763.1:c.-30_-29insAAA | NP_001012781.1:n.-30_-29insAAA | |
| NM_000406.3:c.-30_-29insAAA MANE Select | NP_000397.1:n.-30_-29insAAA | |
| NM_001012763.2:c.-30_-29insAAA | NP_001012781.1:n.-30_-29insAAA |