Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48510042del , CM000677.2:g.48510042del | GRCh38 |
| NC_000015.9:g.48802239del , CM000677.1:g.48802239del | GRCh37 |
| NC_000015.8:g.46589531del | NCBI36 |
| NG_008805.2:g.140747del , LRG_778:g.140747del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000559133.6:c.1714+2del | ENSP00000453958.2:n.1714+2del | |
| ENST00000674301.2:c.1714+2del | ENSP00000501333.2:n.1714+2del | |
| ENST00000684448.1:n.388+2del | ||
| ENST00000316623.10:c.1714+2del MANE Select | ENSP00000325527.5:n.1714+2del | |
| ENST00000316623.9:c.1714+2del | ENSP00000325527.5:n.1714+2del | |
| ENST00000537463.6:c.636+27669del | ENSP00000440294.2:n.636+27669del | |
| NM_000138.4:c.1714+2del , LRG_778t1:c.1714+2del | NP_000129.3:n.1714+2del | |
| NM_000138.5:c.1714+2del MANE Select | NP_000129.3:n.1714+2del |