Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965958_37966009del , CM000670.2:g.37965958_37966009del | GRCh38 |
| NC_000008.10:g.37823476_37823527del , CM000670.1:g.37823476_37823527del | GRCh37 |
| NC_000008.9:g.37942633_37942684del | NCBI36 |
| NG_011936.1:g.5658_5709del |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000025.3:c.461_512del MANE Select | NP_000016.1:p.Ala154GlyfsTer4 |
| ENST00000345060.5:c.461_512del MANE Select | ENSP00000343782.3:p.Ala154GlyfsTer4 |
| NM_000025.2:c.461_512del | NP_000016.1:p.Ala154GlyfsTer4 |
| ENST00000345060.4:c.461_512del | ENSP00000343782.3:p.Ala154GlyfsTer4 |
| ENST00000520341.2:n.589_640del | |
| ENST00000614635.1:c.461_512del | ENSP00000480325.1:p.Ala154GlyfsTer4 |