Linked Data
ClinVar Variation Id:
44802
ClinVar RCV Id:
RCV000037918
dbSNP Id:
rs397516890
COSMIC:
COSM6022225
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140781601_140781603del , CM000669.2:g.140781601_140781603del | GRCh38 |
| NC_000007.13:g.140481401_140481403del , CM000669.1:g.140481401_140481403del | GRCh37 |
| NC_000007.12:g.140127870_140127872del | NCBI36 |
| NG_007873.3:g.148162_148164del , LRG_299:g.148162_148164del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000646891.2:c.1405_1407del MANE Select | ENSP00000493543.1:p.Gly469del | |
| ENST00000288602.11:c.1525_1527del | ENSP00000288602.7:p.Gly509del | |
| ENST00000479537.6:c.75_77del | ||
| ENST00000496384.7:c.1405_1407del | ENSP00000419060.2:p.Gly469del | |
| ENST00000497784.2:c.*855_*857del | ENSP00000420119.2:n.*855_*857del | |
| ENST00000642228.1:c.*483_*485del | ENSP00000493678.1:n.*483_*485del | |
| ENST00000642875.1:n.847_849del | ||
| ENST00000644120.1:n.1795_1797del | ||
| ENST00000644650.1:c.501_503del | ||
| ENST00000644905.1:n.1494_1496del | ||
| ENST00000644969.2:c.1525_1527del MANE Plus Clinical | ENSP00000496776.1:p.Gly509del | |
| ENST00000646334.1:n.535_537del | ||
| ENST00000646730.1:c.1405_1407del | ENSP00000494784.1:p.Gly469del | |
| ENST00000646891.1:c.1405_1407del | ENSP00000493543.1:p.Gly469del | |
| ENST00000647434.1:c.448_450del | ENSP00000495132.1:p.Gly150del | |
| ENST00000288602.10:c.1405_1407del | ENSP00000288602.6:p.Gly469del | |
| ENST00000496384.6:c.228_230del | ||
| ENST00000497784.1:c.1440_1442del | ENSP00000420119.1:n.1440_1442del | |
| NM_004333.4:c.1405_1407del , LRG_299t1:c.1405_1407del | NP_004324.2:p.Gly469del | |
| XM_005250045.1:c.1405_1407del | XP_005250102.1:p.Gly469del | |
| XM_005250046.1:c.1405_1407del | XP_005250103.1:p.Gly469del | |
| XM_011516529.1:c.1405_1407del | XP_011514831.1:p.Gly469del | |
| XM_011516530.1:c.1405_1407del | XP_011514832.1:p.Gly469del | |
| XR_242190.1:n.1413_1415del | ||
| XR_927520.1:n.1413_1415del | ||
| XR_927521.1:n.1413_1415del | ||
| XR_927522.1:n.1413_1415del | ||
| XR_927523.1:n.1413_1415del | ||
| NM_001354609.1:c.1405_1407del | NP_001341538.1:p.Gly469del | |
| NM_004333.5:c.1405_1407del | NP_004324.2:p.Gly469del | |
| NR_148928.1:n.1710_1712del | ||
| XM_017012558.1:c.1525_1527del | XP_016868047.1:p.Gly509del | |
| XM_017012559.1:c.1525_1527del | XP_016868048.1:p.Gly509del | |
| XR_001744857.1:n.1533_1535del | ||
| XR_001744858.1:n.1533_1535del | ||
| NM_001354609.2:c.1405_1407del | NP_001341538.1:p.Gly469del | |
| NM_001374244.1:c.1525_1527del | NP_001361173.1:p.Gly509del | |
| NM_001374258.1:c.1525_1527del MANE Plus Clinical | NP_001361187.1:p.Gly509del | |
| NM_004333.6:c.1405_1407del MANE Select | NP_004324.2:p.Gly469del | |
| NM_001378467.1:c.1414_1416del | NP_001365396.1:p.Gly472del | |
| NM_001378468.1:c.1405_1407del | NP_001365397.1:p.Gly469del | |
| NM_001378469.1:c.1339_1341del | NP_001365398.1:p.Gly447del | |
| NM_001378470.1:c.1303_1305del | NP_001365399.1:p.Gly435del | |
| NM_001378471.1:c.1294_1296del | NP_001365400.1:p.Gly432del | |
| NM_001378472.1:c.1249_1251del | NP_001365401.1:p.Gly417del | |
| NM_001378473.1:c.1249_1251del | NP_001365402.1:p.Gly417del | |
| NM_001378474.1:c.1405_1407del | NP_001365403.1:p.Gly469del | |
| NM_001378475.1:c.1141_1143del | NP_001365404.1:p.Gly381del |