Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10643830del , CM000682.2:g.10643830del | GRCh38 |
| NC_000020.10:g.10624478del , CM000682.1:g.10624478del | GRCh37 |
| NC_000020.9:g.10572478del | NCBI36 |
| NG_007496.1:g.35217del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.2406del MANE Select | ENSP00000254958.4:p.Trp803GlyfsTer17 | |
| ENST00000617965.2:n.2995del | ||
| ENST00000254958.9:c.2406del | ENSP00000254958.4:p.Trp803GlyfsTer17 | |
| ENST00000423891.6:n.2272del | ||
| NM_000214.2:c.2406del | NP_000205.1:p.Trp803GlyfsTer17 | |
| NM_000214.3:c.2406del MANE Select | NP_000205.1:p.Trp803GlyfsTer17 |