Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23422254_23422286del , CM000676.2:g.23422254_23422286del | GRCh38 |
| NC_000014.8:g.23891463_23891495del , CM000676.1:g.23891463_23891495del | GRCh37 |
| NC_000014.7:g.22961303_22961335del | NCBI36 |
| NG_007884.1:g.18382_18414del , LRG_384:g.18382_18414del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.3145_3177del MANE Select | ENSP00000347507.3:p.Glu1049_Leu1059del | |
| ENST00000355349.3:c.3145_3177del | ENSP00000347507.3:p.Glu1049_Leu1059del | |
| NM_000257.3:c.3145_3177del | NP_000248.2:p.Glu1049_Leu1059del | |
| XR_245686.3:n.3251_3283del | ||
| XM_017021340.1:c.3145_3177del | XP_016876829.1:p.Glu1049_Leu1059del | |
| NM_000257.4:c.3145_3177del MANE Select | NP_000248.2:p.Glu1049_Leu1059del |