Linked Data
gnomAD v4:
17-4933276-ATGCAACTGTGAGATC-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4933277_4933291del , CM000679.2:g.4933277_4933291del | GRCh38 |
| NC_000017.10:g.4836572_4836586del , CM000679.1:g.4836572_4836586del | GRCh37 |
| NC_000017.9:g.4777352_4777366del | NCBI36 |
| NG_008767.2:g.5983_5997del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329125.6:c.673_687del (GP1BA) MANE Select | ENSP00000329380.5:p.Cys225_Ile229del | |
| ENST00000649830.1:c.-888+1051_-888+1065del (CHRNE) | ENSP00000496907.1:n.-888+1051_-888+1065del | |
| ENST00000329125.5:c.673_687del (GP1BA) | ENSP00000329380.5:p.Cys225_Ile229del | |
| ENST00000611961.1:c.673_687del (GP1BA) | ENSP00000484439.1:p.Cys225_Ile229del | |
| NM_000173.6:c.673_687del (GP1BA) | NP_000164.5:p.Cys225_Ile229del | |
| NM_000173.7:c.673_687del (GP1BA) MANE Select | NP_000164.5:p.Cys225_Ile229del |