Linked Data
dbSNP Id:
rs1476660200
gnomAD v2:
12-24981463-CAAT-C
gnomAD v3:
12-24828529-CAAT-C
gnomAD v4:
12-24828529-CAAT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.24828534_24828536del , CM000674.2:g.24828534_24828536del | GRCh38 |
| NC_000012.11:g.24981468_24981470del , CM000674.1:g.24981468_24981470del | GRCh37 |
| NC_000012.10:g.24872735_24872737del | NCBI36 |
| NG_008170.1:g.125843_125845del | |
| NG_008170.2:g.125843_125845del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261192.12:c.1119+1291_1119+1293del MANE Select | ENSP00000261192.7:n.1119+1291_1119+1293de... | |
| ENST00000261192.11:c.1119+1291_1119+1293del | ENSP00000261192.7:n.1119+1291_1119+1293de... | |
| ENST00000342945.9:c.936+1291_936+1293del | ENSP00000339805.5:n.936+1291_936+1293del | |
| ENST00000538118.5:c.1116+1291_1116+1293del | ENSP00000440817.1:n.1116+1291_1116+1293de... | |
| ENST00000539282.5:c.1155+1291_1155+1293del | ENSP00000443459.1:n.1155+1291_1155+1293de... | |
| ENST00000539780.5:c.1008+1291_1008+1293del | ENSP00000440827.1:n.1008+1291_1008+1293de... | |
| ENST00000543099.1:n.174+1291_174+1293del | ||
| NM_001178091.1:c.1008+1291_1008+1293del | NP_001171562.1:n.1008+1291_1008+1293del | |
| NM_001178092.1:c.936+1291_936+1293del | NP_001171563.1:n.936+1291_936+1293del | |
| NM_001178093.1:c.1155+1291_1155+1293del | NP_001171564.1:n.1155+1291_1155+1293del | |
| NM_001178094.1:c.1116+1291_1116+1293del | NP_001171565.1:n.1116+1291_1116+1293del | |
| NM_005504.6:c.1119+1291_1119+1293del | NP_005495.2:n.1119+1291_1119+1293del | |
| XM_011520810.1:c.1155+1291_1155+1293del | XP_011519112.1:n.1155+1291_1155+1293del | |
| XR_931441.1:n.1532-2167_1532-2165del | ||
| XR_931442.1:n.1532-2167_1532-2165del | ||
| XR_931443.1:n.1439-2167_1439-2165del | ||
| XM_017019768.2:c.1221+1291_1221+1293del | XP_016875257.1:n.1221+1291_1221+1293del | |
| XR_001748835.2:n.4171+1291_4171+1293del | ||
| XR_001749047.1:n.3978-2167_3978-2165del | ||
| XR_001749048.2:n.3978-2167_3978-2165del | ||
| XR_001749049.1:n.3885-2167_3885-2165del | ||
| NM_005504.7:c.1119+1291_1119+1293del MANE Select | NP_005495.2:n.1119+1291_1119+1293del | |
| NM_001178091.2:c.1008+1291_1008+1293del | NP_001171562.1:n.1008+1291_1008+1293del | |
| NM_001178092.2:c.936+1291_936+1293del | NP_001171563.1:n.936+1291_936+1293del | |
| NM_001178093.2:c.1155+1291_1155+1293del | NP_001171564.1:n.1155+1291_1155+1293del | |
| NM_001178094.2:c.1116+1291_1116+1293del | NP_001171565.1:n.1116+1291_1116+1293del |