Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119672359del , CM000672.2:g.119672359del | GRCh38 |
| NC_000010.10:g.121431871del , CM000672.1:g.121431871del | GRCh37 |
| NC_000010.9:g.121421861del | NCBI36 |
| NG_016125.1:g.25990del , LRG_742:g.25990del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.612del MANE Select | ENSP00000358081.4:p.Tyr205ThrfsTer6 | |
| ENST00000369085.7:c.612del | ENSP00000358081.3:p.Tyr205ThrfsTer6 | |
| ENST00000450186.1:c.438del | ENSP00000410036.1:p.Tyr147ThrfsTer6 | |
| NM_004281.3:c.612del , LRG_742t1:c.612del | NP_004272.2:p.Tyr205ThrfsTer6 | |
| XM_005270287.1:c.612del | XP_005270344.1:p.Tyr205ThrfsTer6 | |
| XM_005270287.2:c.612del | XP_005270344.1:p.Tyr205ThrfsTer6 | |
| NM_004281.4:c.612del MANE Select | NP_004272.2:p.Tyr205ThrfsTer6 |