Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138946033_138946041del , CM000665.2:g.138946033_138946041del | GRCh38 |
| NC_000003.11:g.138664875_138664883del , CM000665.1:g.138664875_138664883del | GRCh37 |
| NC_000003.10:g.140147565_140147573del | NCBI36 |
| NG_012454.1:g.6102_6110del | |
| NG_029796.1:g.3800_3808del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648323.1:c.684_692del MANE Select | ENSP00000497217.1:p.Ala229_Ala231del | |
| ENST00000330315.3:c.684_692del | ENSP00000333188.3:p.Ala229_Ala231del | |
| NM_023067.3:c.684_692del | NP_075555.1:p.Ala229_Ala231del | |
| NM_023067.4:c.684_692del MANE Select | NP_075555.1:p.Ala229_Ala231del |