Linked Data
dbSNP Id:
rs1225798134
gnomAD v3:
10-87966913-T-TG
gnomAD v4:
10-87966913-T-TG
MyVariant Identifiers:
chr10:g.87966913_87966914insG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87966913_87966914insG , CM000672.2:g.87966913_87966914insG | GRCh38 |
| NC_000010.10:g.89726670_89726671insG , CM000672.1:g.89726670_89726671insG | GRCh37 |
| NC_000010.9:g.89716650_89716651insG | NCBI36 |
| NG_007466.2:g.108475_108476insG , LRG_311:g.108475_108476insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710265.1:c.*1682_*1683insG | ENSP00000518161.1:n.*1682_*1683insG | |
| ENST00000688158.2:n.3388_3389insG | ||
| ENST00000706954.1:c.*1441_*1442insG | ENSP00000516674.1:n.*1441_*1442insG | |
| ENST00000706955.1:c.*2688_*2689insG | ENSP00000516675.1:n.*2688_*2689insG | |
| ENST00000688158.1:c.*2764_*2765insG | ENSP00000509254.1:n.*2764_*2765insG | |
| ENST00000693560.1:c.*1441_*1442insG | ENSP00000509861.1:n.*1441_*1442insG | |
| ENST00000371953.8:c.*1441_*1442insG MANE Select | ENSP00000361021.3:n.*1441_*1442insG | |
| ENST00000371953.7:c.*1441_*1442insG | ENSP00000361021.3:n.*1441_*1442insG | |
| NM_000314.5:c.*1441_*1442insG | NP_000305.3:n.*1441_*1442insG | |
| NM_000314.6:c.*1441_*1442insG | NP_000305.3:n.*1441_*1442insG | |
| NM_001304717.2:c.*1441_*1442insG | NP_001291646.2:n.*1441_*1442insG | |
| NM_001304718.1:c.*1441_*1442insG | NP_001291647.1:n.*1441_*1442insG | |
| XM_006717926.2:c.*1441_*1442insG | XP_006717989.1:n.*1441_*1442insG | |
| XM_011539982.1:c.*1441_*1442insG | XP_011538284.1:n.*1441_*1442insG | |
| XR_945791.1:n.3223_3224insG | ||
| NM_000314.7:c.*1441_*1442insG | NP_000305.3:n.*1441_*1442insG | |
| NM_001304717.5:c.*1441_*1442insG | NP_001291646.4:n.*1441_*1442insG | |
| NM_001304718.2:c.*1441_*1442insG | NP_001291647.1:n.*1441_*1442insG | |
| NM_000314.8:c.*1441_*1442insG MANE Select | NP_000305.3:n.*1441_*1442insG |