Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44960912_44960913delinsGC , CM000679.2:g.44960912_44960913delinsGC | GRCh38 |
| NC_000017.10:g.43038280_43038281delinsGC , CM000679.1:g.43038280_43038281delinsGC | GRCh37 |
| NC_000017.9:g.40393806_40393807delinsGC | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000253407.4:c.598-546_598-545delinsGC (C1QL1) MANE Select | ENSP00000253407.2:n.598-546_598-545delins... | |
| ENST00000678938.1:c.-110+2850_-110+2851delinsGC (NMT1) | ENSP00000503621.1:n.-110+2850_-110+2851de... | |
| ENST00000253407.3:c.598-546_598-545delinsGC (C1QL1) | ENSP00000253407.2:n.598-546_598-545delins... | |
| NM_006688.4:c.598-546_598-545delinsGC (C1QL1) | NP_006679.1:n.598-546_598-545delinsGC | |
| NM_006688.5:c.598-546_598-545delinsGC (C1QL1) MANE Select | NP_006679.1:n.598-546_598-545delinsGC |