Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129529147_129529148insACT , CM000665.2:g.129529147_129529148insACT | GRCh38 |
| NC_000003.11:g.129247990_129247991insACT , CM000665.1:g.129247990_129247991insACT | GRCh37 |
| NC_000003.10:g.130730680_130730681insACT | NCBI36 |
| NG_009115.1:g.5509_5510insACT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.361+53_361+54insACT MANE Select | ENSP00000296271.3:n.361+53_361+54insACT | |
| ENST00000296271.3:c.361+53_361+54insACT | ENSP00000296271.3:n.361+53_361+54insACT | |
| NM_000539.3:c.361+53_361+54insACT MANE Select | NP_000530.1:n.361+53_361+54insACT |