Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129529293_129529294del , CM000665.2:g.129529293_129529294del | GRCh38 |
| NC_000003.11:g.129248136_129248137del , CM000665.1:g.129248136_129248137del | GRCh37 |
| NC_000003.10:g.130730826_130730827del | NCBI36 |
| NG_009115.1:g.5655_5656del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.361+199_361+200del MANE Select | ENSP00000296271.3:n.361+199_361+200del | |
| ENST00000296271.3:c.361+199_361+200del | ENSP00000296271.3:n.361+199_361+200del | |
| NM_000539.3:c.361+199_361+200del MANE Select | NP_000530.1:n.361+199_361+200del |