Linked Data
dbSNP Id:
rs769788275
ExAC:
8:128750669 AGCT / A
gnomAD v2:
8-128750669-AGCT-A
gnomAD v4:
8-127738423-AGCT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127738429_127738431del , CM000670.2:g.127738429_127738431del | GRCh38 |
| NC_000008.10:g.128750675_128750677del , CM000670.1:g.128750675_128750677del | GRCh37 |
| NC_000008.9:g.128819857_128819859del | NCBI36 |
| NG_007161.1:g.7360_7362del | |
| NG_007161.2:g.7996_7998del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000707113.1:c.167_169del | ENSP00000516742.1:p.Leu56del | |
| ENST00000707114.1:c.167_169del | ENSP00000516743.1:p.Leu56del | |
| ENST00000707115.1:c.167_169del | ENSP00000516744.1:p.Leu56del | |
| ENST00000707116.1:c.167_169del | ENSP00000516745.1:p.Leu56del | |
| ENST00000517291.2:c.209_211del | ENSP00000429441.2:p.Leu70del | |
| ENST00000524013.2:c.209_211del | ENSP00000430235.2:p.Leu70del | |
| ENST00000621592.8:c.212_214del MANE Select | ENSP00000478887.2:p.Leu71del | |
| ENST00000651626.1:c.-134_-132del | ENSP00000499182.1:n.-134_-132del | |
| ENST00000652288.1:c.167_169del | ENSP00000499105.1:p.Leu56del | |
| ENST00000259523.10:c.167_169del | ENSP00000259523.6:p.Leu56del | |
| ENST00000377970.6:c.167_169del | ENSP00000367207.3:p.Leu56del | |
| ENST00000517291.1:c.209_211del | ENSP00000429441.1:p.Leu70del | |
| ENST00000520751.1:c.133_135del | ENSP00000430226.1:p.Cys45del | |
| ENST00000524013.1:c.209_211del | ENSP00000430235.1:p.Leu70del | |
| ENST00000613283.1:c.212_214del | ENSP00000479618.1:p.Leu71del | |
| ENST00000621592.5:c.212_214del | ENSP00000478887.1:p.Leu71del | |
| NM_002467.4:c.212_214del | NP_002458.2:p.Leu71del | |
| NM_001354870.1:c.209_211del | NP_001341799.1:p.Leu70del | |
| NM_002467.5:c.212_214del | NP_002458.2:p.Leu71del | |
| NM_002467.6:c.212_214del MANE Select | NP_002458.2:p.Leu71del |