Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39665965_39665966del , CM000679.2:g.39665965_39665966del | GRCh38 |
| NC_000017.10:g.37822218_37822219del , CM000679.1:g.37822218_37822219del | GRCh37 |
| NC_000017.9:g.35075744_35075745del | NCBI36 |
| NG_008892.1:g.5620_5621del , LRG_210:g.5620_5621del | |
| NG_042278.1:g.2985_2986del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.3:c.360_361del MANE Select | ENSP00000312624.2:p.Glu120AspfsTer15 | |
| ENST00000309889.2:c.360_361del | ENSP00000312624.2:p.Glu120AspfsTer15 | |
| ENST00000578283.1:c.288_289del | ENSP00000462787.1:p.Glu96AspfsTer15 | |
| NM_003673.3:c.360_361del , LRG_210t1:c.360_361del | NP_003664.1:p.Glu120AspfsTer15 | |
| NM_003673.4:c.360_361del MANE Select | NP_003664.1:p.Glu120AspfsTer15 |