Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94781681_94781682delinsGT , CM000672.2:g.94781681_94781682delinsGT | GRCh38 |
| NC_000010.10:g.96541438_96541439delinsGT , CM000672.1:g.96541438_96541439delinsGT | GRCh37 |
| NC_000010.9:g.96531428_96531429delinsGT | NCBI36 |
| NG_008384.2:g.23976_23977delinsGT | |
| NG_008384.3:g.24001_24002delinsGT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.643-140_643-139delinsGT MANE Select | ENSP00000360372.3:n.643-140_643-139delinsGT | |
| ENST00000645461.1:n.1696-140_1696-139delinsGT | ||
| ENST00000371321.7:c.643-140_643-139delinsGT | ENSP00000360372.3:n.643-140_643-139delinsGT | |
| ENST00000464755.1:c.1406-140_1406-139delinsGT | ENSP00000483243.1:n.1406-140_1406-139delinsGT | |
| NM_000769.2:c.643-140_643-139delinsGT | NP_000760.1:n.643-140_643-139delinsGT | |
| NM_000769.4:c.643-140_643-139delinsGT MANE Select | NP_000760.1:n.643-140_643-139delinsGT |