Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.23868182_23868184del , CM000663.2:g.23868182_23868184del | GRCh38 |
| NC_000001.10:g.24194672_24194674del , CM000663.1:g.24194672_24194674del | GRCh37 |
| NC_000001.9:g.24067259_24067261del | NCBI36 |
| NG_013346.1:g.5189_5191del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374479.4:c.106_108del MANE Select | ENSP00000363603.3:p.Arg36del | |
| ENST00000374479.3:c.106_108del | ENSP00000363603.3:p.Arg36del | |
| NM_000147.4:c.106_108del | NP_000138.2:p.Arg36del | |
| XM_005245821.1:c.-444_-442del | XP_005245878.1:n.-444_-442del | |
| XM_005245821.3:c.-444_-442del | XP_005245878.1:n.-444_-442del | |
| NM_000147.5:c.106_108del MANE Select | NP_000138.2:p.Arg36del | |
| NR_174379.1:n.110_112del | ||
| NR_174380.1:n.110_112del | ||
| NR_174381.1:n.110_112del | ||
| NR_174382.1:n.110_112del |