Linked Data
dbSNP Id:
rs1393921632
gnomAD v3:
10-87966796-TAG-T
gnomAD v4:
10-87966796-TAG-T
MyVariant Identifiers:
chr10:g.87966797_87966798del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87966799_87966800del , CM000672.2:g.87966799_87966800del | GRCh38 |
| NC_000010.10:g.89726556_89726557del , CM000672.1:g.89726556_89726557del | GRCh37 |
| NC_000010.9:g.89716536_89716537del | NCBI36 |
| NG_007466.2:g.108361_108362del , LRG_311:g.108361_108362del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700029.2:c.*1327_*1328del | ENSP00000514759.2:n.*1327_*1328del | |
| ENST00000710265.1:c.*1568_*1569del | ENSP00000518161.1:n.*1568_*1569del | |
| ENST00000688158.2:n.3274_3275del | ||
| ENST00000688922.2:c.*2369_*2370del | ENSP00000508742.2:n.*2369_*2370del | |
| ENST00000700021.1:c.*1327_*1328del | ENSP00000514757.1:n.*1327_*1328del | |
| ENST00000700022.1:c.*1878_*1879del | ENSP00000514758.1:n.*1878_*1879del | |
| ENST00000700024.1:n.3931_3932del | ||
| ENST00000706954.1:c.*1327_*1328del | ENSP00000516674.1:n.*1327_*1328del | |
| ENST00000706955.1:c.*2574_*2575del | ENSP00000516675.1:n.*2574_*2575del | |
| ENST00000688158.1:c.*2650_*2651del | ENSP00000509254.1:n.*2650_*2651del | |
| ENST00000688308.1:c.*1327_*1328del | ENSP00000508752.1:n.*1327_*1328del | |
| ENST00000688922.1:c.2460_2461del | ||
| ENST00000693560.1:c.*1327_*1328del | ENSP00000509861.1:n.*1327_*1328del | |
| ENST00000371953.8:c.*1327_*1328del MANE Select | ENSP00000361021.3:n.*1327_*1328del | |
| ENST00000371953.7:c.*1327_*1328del | ENSP00000361021.3:n.*1327_*1328del | |
| NM_000314.5:c.*1327_*1328del | NP_000305.3:n.*1327_*1328del | |
| NM_000314.6:c.*1327_*1328del | NP_000305.3:n.*1327_*1328del | |
| NM_001304717.2:c.*1327_*1328del | NP_001291646.2:n.*1327_*1328del | |
| NM_001304718.1:c.*1327_*1328del | NP_001291647.1:n.*1327_*1328del | |
| XM_006717926.2:c.*1327_*1328del | XP_006717989.1:n.*1327_*1328del | |
| XM_011539982.1:c.*1327_*1328del | XP_011538284.1:n.*1327_*1328del | |
| XR_945791.1:n.3109_3110del | ||
| NM_000314.7:c.*1327_*1328del | NP_000305.3:n.*1327_*1328del | |
| NM_001304717.5:c.*1327_*1328del | NP_001291646.4:n.*1327_*1328del | |
| NM_001304718.2:c.*1327_*1328del | NP_001291647.1:n.*1327_*1328del | |
| NM_000314.8:c.*1327_*1328del MANE Select | NP_000305.3:n.*1327_*1328del |