Linked Data
dbSNP Id:
rs1431961300
gnomAD v2:
X-19378140-CGCTGGT-C
gnomAD v3:
X-19360022-CGCTGGT-C
gnomAD v4:
X-19360022-CGCTGGT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.19360027_19360032del , CM000685.2:g.19360027_19360032del | GRCh38 |
| NC_000023.10:g.19378145_19378150del , CM000685.1:g.19378145_19378150del | GRCh37 |
| NC_000023.9:g.19288066_19288071del | NCBI36 |
| NG_016781.1:g.21135_21140del | |
| NG_021184.1:g.160234_160239del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355808.10:c.*374_*379del | ENSP00000348062.6:n.*374_*379del | |
| ENST00000423505.6:c.*374_*379del | ENSP00000406473.2:n.*374_*379del | |
| ENST00000696704.1:c.*879_*884del | ENSP00000512823.1:n.*879_*884del | |
| ENST00000696705.1:c.*1002_*1007del | ENSP00000512824.1:n.*1002_*1007del | |
| ENST00000422285.7:c.*374_*379del MANE Select | ENSP00000394382.2:n.*374_*379del | |
| ENST00000379806.9:c.*374_*379del | ENSP00000369134.5:n.*374_*379del | |
| ENST00000422285.6:c.*374_*379del | ENSP00000394382.2:n.*374_*379del | |
| ENST00000540249.5:c.*374_*379del | ENSP00000440761.1:n.*374_*379del | |
| ENST00000545074.5:c.*374_*379del | ENSP00000438550.1:n.*374_*379del | |
| NM_000284.3:c.*374_*379del | NP_000275.1:n.*374_*379del | |
| NM_001173454.1:c.*374_*379del | NP_001166925.1:n.*374_*379del | |
| NM_001173455.1:c.*374_*379del | NP_001166926.1:n.*374_*379del | |
| NM_001173456.1:c.*374_*379del | NP_001166927.1:n.*374_*379del | |
| XM_011545531.1:c.*374_*379del | XP_011543833.1:n.*374_*379del | |
| XM_011545532.1:c.*374_*379del | XP_011543834.1:n.*374_*379del | |
| NM_000284.4:c.*374_*379del MANE Select | NP_000275.1:n.*374_*379del | |
| NM_001173454.2:c.*374_*379del | NP_001166925.1:n.*374_*379del | |
| NM_001173455.2:c.*374_*379del | NP_001166926.1:n.*374_*379del | |
| NM_001173456.2:c.*374_*379del | NP_001166927.1:n.*374_*379del |