Linked Data
ClinVar Variation Id:
557418
ClinVar RCV Id:
RCV000673560
dbSNP Id:
rs754779351
gnomAD v4:
10-53822445-C-CAGG
MyVariant Identifiers:
chr10:g.53822446_53822448dup (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.53822454_53822456dup , CM000672.2:g.53822454_53822456dup | GRCh38 |
| NC_000010.10:g.55582214_55582216dup , CM000672.1:g.55582214_55582216dup | GRCh37 |
| NC_000010.9:g.55252220_55252222dup | NCBI36 |
| NG_009191.2:g.983844_983846dup | |
| NG_009191.3:g.1811735_1811737dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613657.6:c.4409+2688_4409+2690dup | ENSP00000482794.1:n.4409+2688_4409+2690dup | |
| ENST00000320301.11:c.5278_5280dup MANE Plus Clinical | ENSP00000322604.6:p.Pro1760_Ala1761insPro | |
| ENST00000395445.6:c.4388+4945_4388+4947dup | ENSP00000378832.2:n.4388+4945_4388+4947dup | |
| ENST00000613657.5:c.4409+2688_4409+2690dup | ENSP00000482794.1:n.4409+2688_4409+2690dup | |
| ENST00000642496.1:c.3227-2218_3227-2216dup | ||
| ENST00000644397.2:c.4368-2218_4368-2216dup MANE Select | ENSP00000495195.1:n.4368-2218_4368-2216dup | |
| ENST00000320301.10:c.5278_5280dup | ENSP00000322604.6:p.Pro1760_Ala1761insPro | |
| ENST00000361849.7:c.5284_5286dup | ENSP00000354950.3:p.Pro1762_Ala1763insPro | |
| ENST00000373956.7:c.*3233_*3235dup | ENSP00000363067.4:n.*3233_*3235dup | |
| ENST00000373957.7:c.5299_5301dup | ENSP00000363068.4:p.Pro1767_Ala1768insPro | |
| ENST00000373965.6:c.4373+2688_4373+2690dup | ENSP00000363076.3:n.4373+2688_4373+2690dup | |
| ENST00000395430.5:c.5269_5271dup | ENSP00000378818.1:p.Pro1757_Ala1758insPro | |
| ENST00000395432.6:c.5158_5160dup | ENSP00000378820.2:p.Pro1720_Ala1721insPro | |
| ENST00000395433.5:c.5209_5211dup | ENSP00000378821.1:p.Pro1737_Ala1738insPro | |
| ENST00000395438.5:c.4371+4944_4371+4946dup | ENSP00000378826.2:n.4371+4944_4371+4946dup | |
| ENST00000395440.5:c.1306-12902_1306-12900dup | ENSP00000378827.1:n.1306-12902_1306-12900dup | |
| ENST00000395442.5:c.1099-12902_1099-12900dup | ENSP00000378829.1:n.1099-12902_1099-12900dup | |
| ENST00000395445.5:c.4388+4945_4388+4947dup | ENSP00000378832.2:n.4388+4945_4388+4947dup | |
| ENST00000395446.5:c.2092-12902_2092-12900dup | ENSP00000378833.1:n.2092-12902_2092-12900dup | |
| ENST00000409834.5:c.3206+2688_3206+2690dup | ENSP00000386693.1:n.3206+2688_3206+2690dup | |
| ENST00000414367.5:c.*447+4945_*447+4947dup | ENSP00000412531.1:n.*447+4945_*447+4947dup | |
| ENST00000414778.5:c.4370+4945_4370+4947dup | ENSP00000410304.2:n.4370+4945_4370+4947dup | |
| ENST00000437009.5:c.5071_5073dup | ENSP00000412628.2:p.Pro1691_Ala1692insPro | |
| ENST00000448885.5:c.*3239_*3241dup | ENSP00000412320.1:n.*3239_*3241dup | |
| ENST00000463095.2:n.2297_2299dup | ||
| ENST00000495484.5:c.462-4435_462-4433dup | ENSP00000480780.1:n.462-4435_462-4433dup | |
| ENST00000612394.4:c.4406+4945_4406+4947dup | ENSP00000482921.1:n.4406+4945_4406+4947dup | |
| ENST00000613657.4:c.4409+2688_4409+2690dup | ENSP00000482794.1:n.4409+2688_4409+2690dup | |
| ENST00000614895.4:c.4385+4945_4385+4947dup | ENSP00000478512.1:n.4385+4945_4385+4947dup | |
| ENST00000616114.4:c.4367+4945_4367+4947dup | ENSP00000483745.1:n.4367+4945_4367+4947dup | |
| ENST00000617051.4:c.5305_5307dup | ENSP00000484703.1:p.Pro1769_Ala1770insPro | |
| ENST00000617271.4:c.4373+2688_4373+2690dup | ENSP00000478076.1:n.4373+2688_4373+2690dup | |
| ENST00000618301.4:c.594-4435_594-4433dup | ENSP00000482780.1:n.594-4435_594-4433dup | |
| ENST00000621708.4:c.4388+2688_4388+2690dup | ENSP00000484454.1:n.4388+2688_4388+2690dup | |
| ENST00000622048.4:c.5077_5079dup | ENSP00000482329.1:p.Pro1693_Ala1694insPro | |
| NM_001142763.1:c.5299_5301dup | NP_001136235.1:p.Pro1767_Ala1768insPro | |
| NM_001142764.1:c.5284_5286dup | NP_001136236.1:p.Pro1762_Ala1763insPro | |
| NM_001142765.1:c.5071_5073dup | NP_001136237.1:p.Pro1691_Ala1692insPro | |
| NM_001142766.1:c.5269_5271dup | NP_001136238.1:p.Pro1757_Ala1758insPro | |
| NM_001142767.1:c.5158_5160dup | NP_001136239.1:p.Pro1720_Ala1721insPro | |
| NM_001142768.1:c.5218_5220dup | NP_001136240.1:p.Pro1740_Ala1741insPro | |
| NM_001142769.1:c.4409+2688_4409+2690dup | NP_001136241.1:n.4409+2688_4409+2690dup | |
| NM_001142770.1:c.4373+2688_4373+2690dup | NP_001136242.1:n.4373+2688_4373+2690dup | |
| NM_001142771.1:c.4388+2688_4388+2690dup | NP_001136243.1:n.4388+2688_4388+2690dup | |
| NM_001142772.1:c.4373+2688_4373+2690dup | NP_001136244.1:n.4373+2688_4373+2690dup | |
| NM_001142773.1:c.5209_5211dup | NP_001136245.1:p.Pro1737_Ala1738insPro | |
| NM_033056.3:c.5278_5280dup | NP_149045.3:p.Pro1760_Ala1761insPro | |
| NM_001142769.2:c.4409+2688_4409+2690dup | NP_001136241.1:n.4409+2688_4409+2690dup | |
| NM_001142770.2:c.4373+2688_4373+2690dup | NP_001136242.1:n.4373+2688_4373+2690dup | |
| NM_001354404.1:c.5212_5214dup | NP_001341333.1:p.Pro1738_Ala1739insPro | |
| NM_001354411.1:c.4388+4945_4388+4947dup | NP_001341340.1:n.4388+4945_4388+4947dup | |
| NM_001354420.1:c.4367+4945_4367+4947dup | NP_001341349.1:n.4367+4945_4367+4947dup | |
| NM_001354429.1:c.4368-4435_4368-4433dup | NP_001341358.1:n.4368-4435_4368-4433dup | |
| XM_017016573.2:c.4388+2688_4388+2690dup | XP_016872062.1:n.4388+2688_4388+2690dup | |
| XR_001747192.2:n.6291_6293dup | ||
| XR_001747193.2:n.6282_6284dup | ||
| NM_001142763.2:c.5299_5301dup | NP_001136235.1:p.Pro1767_Ala1768insPro | |
| NM_001142764.2:c.5284_5286dup | NP_001136236.1:p.Pro1762_Ala1763insPro | |
| NM_001142765.2:c.5071_5073dup | NP_001136237.1:p.Pro1691_Ala1692insPro | |
| NM_001142766.2:c.5269_5271dup | NP_001136238.1:p.Pro1757_Ala1758insPro | |
| NM_001142768.2:c.5218_5220dup | NP_001136240.1:p.Pro1740_Ala1741insPro | |
| NM_001142769.3:c.4409+2688_4409+2690dup | NP_001136241.1:n.4409+2688_4409+2690dup | |
| NM_001142770.3:c.4373+2688_4373+2690dup | NP_001136242.1:n.4373+2688_4373+2690dup | |
| NM_001142771.2:c.4388+2688_4388+2690dup | NP_001136243.1:n.4388+2688_4388+2690dup | |
| NM_001142772.2:c.4373+2688_4373+2690dup | NP_001136244.1:n.4373+2688_4373+2690dup | |
| NM_001142773.2:c.5209_5211dup | NP_001136245.1:p.Pro1737_Ala1738insPro | |
| NM_001354411.2:c.4388+4945_4388+4947dup | NP_001341340.1:n.4388+4945_4388+4947dup | |
| NM_001354420.2:c.4367+4945_4367+4947dup | NP_001341349.1:n.4367+4945_4367+4947dup | |
| NM_001354429.2:c.4368-4435_4368-4433dup | NP_001341358.1:n.4368-4435_4368-4433dup | |
| NM_033056.4:c.5278_5280dup MANE Plus Clinical | NP_149045.3:p.Pro1760_Ala1761insPro | |
| NM_001142767.2:c.5158_5160dup | NP_001136239.1:p.Pro1720_Ala1721insPro | |
| NM_001354404.2:c.5212_5214dup | NP_001341333.1:p.Pro1738_Ala1739insPro | |
| NM_001384140.1:c.4368-2218_4368-2216dup MANE Select | NP_001371069.1:n.4368-2218_4368-2216dup |