Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184059998del , CM000665.2:g.184059998del | GRCh38 |
| NC_000003.11:g.183777786del , CM000665.1:g.183777786del | GRCh37 |
| NC_000003.10:g.185260480del | NCBI36 |
| NG_012749.1:g.11952del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318351.2:c.1096del MANE Select | ENSP00000322617.1:p.Gln366ArgfsTer23 | |
| ENST00000318351.1:c.1096del | ENSP00000322617.1:p.Gln366ArgfsTer23 | |
| NM_130770.2:c.1096del | NP_570126.2:p.Gln366ArgfsTer23 | |
| NM_130770.3:c.1096del MANE Select | NP_570126.2:p.Gln366ArgfsTer23 |