Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4933112_4933116delinsAGTCT , CM000679.2:g.4933112_4933116delinsAGTCT | GRCh38 |
| NC_000017.10:g.4836407_4836411delinsAGTCT , CM000679.1:g.4836407_4836411delinsAGTCT | GRCh37 |
| NC_000017.9:g.4777187_4777191delinsAGTCT | NCBI36 |
| NG_008767.2:g.5818_5822delinsAGTCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329125.6:c.508_512delinsAGTCT (GP1BA) MANE Select | ENSP00000329380.5:p.Ser170= | |
| ENST00000649830.1:c.-888+1226_-888+1230delinsAGACT (CHRNE) | ENSP00000496907.1:n.-888+1226_-888+1230delinsAGACT | |
| ENST00000329125.5:c.508_512delinsAGTCT (GP1BA) | ENSP00000329380.5:p.Ser170= | |
| ENST00000611961.1:c.508_512delinsAGTCT (GP1BA) | ENSP00000484439.1:p.Ser170= | |
| NM_000173.6:c.508_512delinsAGTCT (GP1BA) | NP_000164.5:p.Ser170= | |
| NM_000173.7:c.508_512delinsAGTCT (GP1BA) MANE Select | NP_000164.5:p.Ser170= |