| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965731dup , CM000670.2:g.37965731dup | GRCh38 |
| NC_000008.10:g.37823249dup , CM000670.1:g.37823249dup | GRCh37 |
| NC_000008.9:g.37942406dup | NCBI36 |
| NG_011936.1:g.5938dup |
| HGVS | Amino-acid Change |
|---|---|
| NM_000025.3:c.741dup MANE Select | NP_000016.1:p.Glu248ArgfsTer? |
| ENST00000345060.5:c.741dup MANE Select | ENSP00000343782.3:p.Glu248ArgfsTer? |
| NM_000025.2:c.741dup | NP_000016.1:p.Glu248ArgfsTer? |
| ENST00000345060.4:c.741dup | ENSP00000343782.3:p.Glu248ArgfsTer? |
| ENST00000520341.1:n.16dup | |
| ENST00000520341.2:n.869dup | |
| ENST00000614635.1:c.741dup | ENSP00000480325.1:p.Glu248ArgfsTer? |
| ENST00000647937.1:c.225dup | ENSP00000497740.1:p.Glu76ArgfsTer? |