Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119676621del , CM000672.2:g.119676621del | GRCh38 |
| NC_000010.10:g.121436133del , CM000672.1:g.121436133del | GRCh37 |
| NC_000010.9:g.121426123del | NCBI36 |
| NG_016125.1:g.30252del , LRG_742:g.30252del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000369085.8:c.1067del MANE Select | ENSP00000358081.4:p.Pro356HisfsTer7 | |
| ENST00000369085.7:c.1067del | ENSP00000358081.3:p.Pro356HisfsTer7 | |
| ENST00000450186.1:c.890del | ENSP00000410036.1:p.Pro297HisfsTer7 | |
| NM_004281.3:c.1067del , LRG_742t1:c.1067del | NP_004272.2:p.Pro356HisfsTer7 | |
| XM_005270287.1:c.1064del | XP_005270344.1:p.Pro355HisfsTer7 | |
| XM_005270287.2:c.1064del | XP_005270344.1:p.Pro355HisfsTer7 | |
| NM_004281.4:c.1067del MANE Select | NP_004272.2:p.Pro356HisfsTer7 |