Linked Data
dbSNP Id:
rs556734672
gnomAD v2:
14-65569163-ACACTCACTCACT-A
gnomAD v3:
14-65102445-ACACTCACTCACT-A
gnomAD v4:
14-65102445-ACACTCACTCACT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.65102455_65102466del , CM000676.2:g.65102455_65102466del | GRCh38 |
| NC_000014.8:g.65569173_65569184del , CM000676.1:g.65569173_65569184del | GRCh37 |
| NC_000014.7:g.64638926_64638937del | NCBI36 |
| NG_029830.1:g.5053_5064del , LRG_530:g.5053_5064del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000556892.6:c.-157+52_-157+63del | ENSP00000452206.2:n.-157+52_-157+63del | |
| ENST00000556979.6:c.-118_-107del | ENSP00000452378.1:n.-118_-107del | |
| ENST00000358664.9:c.-118_-107del MANE Select | ENSP00000351490.4:n.-118_-107del | |
| ENST00000246163.2:c.-118_-107del | ENSP00000246163.2:n.-118_-107del | |
| ENST00000284165.10:c.-118_-107del | ENSP00000284165.6:n.-118_-107del | |
| ENST00000358402.8:c.-118_-107del | ENSP00000351175.4:n.-118_-107del | |
| ENST00000358664.8:c.-118_-107del | ENSP00000351490.4:n.-118_-107del | |
| ENST00000394606.6:c.-118_-107del | ENSP00000378104.2:n.-118_-107del | |
| ENST00000554709.1:n.61_72del | ||
| ENST00000555667.5:c.-118_-107del | ENSP00000452286.1:n.-118_-107del | |
| ENST00000555932.5:c.-118_-107del | ENSP00000450763.1:n.-118_-107del | |
| ENST00000556443.5:c.-118_-107del | ENSP00000450818.1:n.-118_-107del | |
| ENST00000556702.1:n.22_33del | ||
| ENST00000556892.5:c.-157+52_-157+63del | ENSP00000452206.1:n.-157+52_-157+63del | |
| ENST00000556979.5:c.-118_-107del | ENSP00000452378.1:n.-118_-107del | |
| ENST00000557277.5:c.-239+52_-239+63del | ENSP00000450955.1:n.-239+52_-239+63del | |
| ENST00000557746.5:c.-118_-107del | ENSP00000452197.1:n.-118_-107del | |
| ENST00000618858.4:c.-118_-107del | ENSP00000480127.1:n.-118_-107del | |
| NM_001271068.1:c.-118_-107del | NP_001257997.1:n.-118_-107del | |
| NM_001271069.1:c.-118_-107del | NP_001257998.1:n.-118_-107del | |
| NM_002382.4:c.-118_-107del | NP_002373.3:n.-118_-107del | |
| NM_145112.2:c.-118_-107del | NP_660087.1:n.-118_-107del | |
| NM_145113.2:c.-118_-107del | NP_660088.1:n.-118_-107del | |
| NM_145114.2:c.-118_-107del | NP_660089.1:n.-118_-107del | |
| NM_197957.3:c.-118_-107del | NP_932061.1:n.-118_-107del | |
| NR_073137.1:n.187+52_187+63del | ||
| NR_073138.1:n.187+52_187+63del | ||
| XM_011536773.1:c.-118_-107del | XP_011535075.1:n.-118_-107del | |
| XR_429315.2:n.85_96del | ||
| XR_943450.1:n.85_96del | ||
| XR_943451.1:n.85_96del | ||
| XR_943452.1:n.74_85del | ||
| NM_001320415.1:c.-392_-381del | NP_001307344.1:n.-392_-381del | |
| XM_011536773.3:c.-118_-107del | XP_011535075.1:n.-118_-107del | |
| XM_017021312.2:c.-365_-354del | XP_016876801.1:n.-365_-354del | |
| XR_001750326.2:n.73_84del | ||
| XR_001750327.2:n.73_84del | ||
| XR_002957553.1:n.76_87del | ||
| XR_943450.3:n.85_96del | ||
| XR_943451.3:n.85_96del | ||
| XR_943452.3:n.73_84del | ||
| NM_001320415.2:c.-392_-381del | NP_001307344.1:n.-392_-381del | |
| NM_002382.5:c.-118_-107del MANE Select | NP_002373.3:n.-118_-107del | |
| NM_145112.3:c.-118_-107del | NP_660087.1:n.-118_-107del | |
| NM_145113.3:c.-118_-107del | NP_660088.1:n.-118_-107del | |
| NM_001271068.2:c.-118_-107del | NP_001257997.1:n.-118_-107del | |
| NM_001271069.2:c.-118_-107del | NP_001257998.1:n.-118_-107del | |
| NM_145114.3:c.-118_-107del | NP_660089.1:n.-118_-107del | |
| NM_197957.4:c.-118_-107del | NP_932061.1:n.-118_-107del |