Linked Data
dbSNP Id:
rs1264793381
gnomAD v2:
14-21883692-AT-A
gnomAD v3:
14-21415533-AT-A
gnomAD v4:
14-21415533-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.21415534del , CM000676.2:g.21415534del | GRCh38 |
| NC_000014.8:g.21883693del , CM000676.1:g.21883693del | GRCh37 |
| NC_000014.7:g.20953533del | NCBI36 |
| NG_021249.1:g.26765del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000430710.8:c.1131+40del | ENSP00000406288.3:n.1131+40del | |
| ENST00000555962.6:c.-110-12492del | ENSP00000495174.1:n.-110-12492del | |
| ENST00000557364.6:c.1968+40del | ENSP00000451601.1:n.1968+40del | |
| ENST00000642914.1:n.991del | ||
| ENST00000643469.1:c.1968+40del | ENSP00000495070.1:n.1968+40del | |
| ENST00000645140.1:c.1880+40del | ||
| ENST00000645206.1:n.482+40del | ||
| ENST00000645929.1:c.1131+40del | ENSP00000494402.1:n.1131+40del | |
| ENST00000646340.1:c.1974+40del | ENSP00000496730.1:n.1974+40del | |
| ENST00000646647.2:c.1968+40del MANE Select | ENSP00000495240.1:n.1968+40del | |
| ENST00000399982.6:c.1968+40del | ENSP00000382863.2:n.1968+40del | |
| ENST00000430710.7:c.1131+40del | ENSP00000406288.3:n.1131+40del | |
| ENST00000555962.5:n.151-12492del | ||
| ENST00000557364.5:c.1968+40del | ENSP00000451601.1:n.1968+40del | |
| NM_001170629.1:c.1968+40del | NP_001164100.1:n.1968+40del | |
| NM_020920.3:c.1131+40del | NP_065971.2:n.1131+40del | |
| NM_001170629.2:c.1968+40del MANE Select | NP_001164100.1:n.1968+40del | |
| NM_020920.4:c.1131+40del | NP_065971.2:n.1131+40del |