Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119669922_119669928dup , CM000672.2:g.119669922_119669928dup | GRCh38 |
| NC_000010.10:g.121429434_121429440dup , CM000672.1:g.121429434_121429440dup | GRCh37 |
| NC_000010.9:g.121419424_121419430dup | NCBI36 |
| NG_016125.1:g.23553_23559dup , LRG_742:g.23553_23559dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.252_258dup MANE Select | ENSP00000358081.4:p.Pro87CysfsTer17 | |
| ENST00000369085.7:c.252_258dup | ENSP00000358081.3:p.Pro87CysfsTer17 | |
| ENST00000450186.1:c.78_84dup | ENSP00000410036.1:p.Pro29CysfsTer17 | |
| NM_004281.3:c.252_258dup , LRG_742t1:c.252_258dup | NP_004272.2:p.Pro87CysfsTer17 | |
| XM_005270287.1:c.252_258dup | XP_005270344.1:p.Pro87CysfsTer17 | |
| XM_005270287.2:c.252_258dup | XP_005270344.1:p.Pro87CysfsTer17 | |
| NM_004281.4:c.252_258dup MANE Select | NP_004272.2:p.Pro87CysfsTer17 |