Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67754092_67754093del , CM000666.2:g.67754092_67754093del | GRCh38 |
| NC_000004.11:g.68619810_68619811del , CM000666.1:g.68619810_68619811del | GRCh37 |
| NC_000004.10:g.68302405_68302406del | NCBI36 |
| NG_009293.1:g.6995_6996del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226413.5:c.244_245del MANE Select | ENSP00000226413.5:p.His82SerfsTer? | |
| ENST00000226413.4:c.244_245del | ENSP00000226413.4:p.His82SerfsTer? | |
| ENST00000420975.2:c.244_245del | ENSP00000397561.2:p.His82SerfsTer? | |
| NM_000406.2:c.244_245del | NP_000397.1:p.His82SerfsTer? | |
| NM_001012763.1:c.244_245del | NP_001012781.1:p.His82SerfsTer? | |
| NM_000406.3:c.244_245del MANE Select | NP_000397.1:p.His82SerfsTer? | |
| NM_001012763.2:c.244_245del | NP_001012781.1:p.His82SerfsTer? |