Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240878783del , CM000664.2:g.240878783del | GRCh38 |
| NC_000002.11:g.241818200del , CM000664.1:g.241818200del | GRCh37 |
| NC_000002.10:g.241466873del | NCBI36 |
| NG_008005.1:g.15039del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.1141del MANE Select | ENSP00000302620.3:p.Arg381GlyfsTer? | |
| ENST00000307503.3:c.1141del | ENSP00000302620.3:p.Arg381GlyfsTer? | |
| ENST00000470255.1:n.919del | ||
| NM_000030.2:c.1141del | NP_000021.1:p.Arg381GlyfsTer? | |
| NM_000030.3:c.1141del MANE Select | NP_000021.1:p.Arg381GlyfsTer? |