Linked Data
ClinVar Variation Id:
432938
dbSNP Id:
rs774056663
gnomAD v2:
10-55583016-A-AATAGTATT
gnomAD v3:
10-53823256-A-AATAGTATT
gnomAD v4:
10-53823256-A-AATAGTATT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.53823257_53823264dup , CM000672.2:g.53823257_53823264dup | GRCh38 |
| NC_000010.10:g.55583017_55583024dup , CM000672.1:g.55583017_55583024dup | GRCh37 |
| NC_000010.9:g.55253023_55253030dup | NCBI36 |
| NG_009191.2:g.983028_983035dup | |
| NG_009191.3:g.1810919_1810926dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613657.6:c.4409+1872_4409+1879dup | ENSP00000482794.1:n.4409+1872_4409+1879dup | |
| ENST00000320301.11:c.4462_4469dup MANE Plus Clinical | ENSP00000322604.6:p.Glu1491IlefsTer11 | |
| ENST00000395445.6:c.4388+4129_4388+4136dup | ENSP00000378832.2:n.4388+4129_4388+4136dup | |
| ENST00000613657.5:c.4409+1872_4409+1879dup | ENSP00000482794.1:n.4409+1872_4409+1879dup | |
| ENST00000642496.1:c.3227-3034_3227-3027dup | ||
| ENST00000644397.2:c.4368-3034_4368-3027dup MANE Select | ENSP00000495195.1:n.4368-3034_4368-3027dup | |
| ENST00000320301.10:c.4462_4469dup | ENSP00000322604.6:p.Glu1491IlefsTer11 | |
| ENST00000361849.7:c.4468_4475dup | ENSP00000354950.3:p.Glu1493IlefsTer11 | |
| ENST00000373956.7:c.*2417_*2424dup | ENSP00000363067.4:n.*2417_*2424dup | |
| ENST00000373957.7:c.4483_4490dup | ENSP00000363068.4:p.Glu1498IlefsTer11 | |
| ENST00000373965.6:c.4373+1872_4373+1879dup | ENSP00000363076.3:n.4373+1872_4373+1879dup | |
| ENST00000395430.5:c.4453_4460dup | ENSP00000378818.1:p.Glu1488IlefsTer11 | |
| ENST00000395432.6:c.4342_4349dup | ENSP00000378820.2:p.Glu1451IlefsTer11 | |
| ENST00000395433.5:c.4393_4400dup | ENSP00000378821.1:p.Glu1468IlefsTer11 | |
| ENST00000395438.5:c.4371+4128_4371+4135dup | ENSP00000378826.2:n.4371+4128_4371+4135dup | |
| ENST00000395440.5:c.1306-13718_1306-13711dup | ENSP00000378827.1:n.1306-13718_1306-13711dup | |
| ENST00000395442.5:c.1099-13718_1099-13711dup | ENSP00000378829.1:n.1099-13718_1099-13711dup | |
| ENST00000395445.5:c.4388+4129_4388+4136dup | ENSP00000378832.2:n.4388+4129_4388+4136dup | |
| ENST00000395446.5:c.2092-13718_2092-13711dup | ENSP00000378833.1:n.2092-13718_2092-13711dup | |
| ENST00000409834.5:c.3206+1872_3206+1879dup | ENSP00000386693.1:n.3206+1872_3206+1879dup | |
| ENST00000414367.5:c.*447+4129_*447+4136dup | ENSP00000412531.1:n.*447+4129_*447+4136dup | |
| ENST00000414778.5:c.4370+4129_4370+4136dup | ENSP00000410304.2:n.4370+4129_4370+4136dup | |
| ENST00000437009.5:c.4255_4262dup | ENSP00000412628.2:p.Glu1422IlefsTer11 | |
| ENST00000448885.5:c.*2423_*2430dup | ENSP00000412320.1:n.*2423_*2430dup | |
| ENST00000463095.2:n.1481_1488dup | ||
| ENST00000495484.5:c.462-5251_462-5244dup | ENSP00000480780.1:n.462-5251_462-5244dup | |
| ENST00000612394.4:c.4406+4129_4406+4136dup | ENSP00000482921.1:n.4406+4129_4406+4136dup | |
| ENST00000613657.4:c.4409+1872_4409+1879dup | ENSP00000482794.1:n.4409+1872_4409+1879dup | |
| ENST00000614895.4:c.4385+4129_4385+4136dup | ENSP00000478512.1:n.4385+4129_4385+4136dup | |
| ENST00000616114.4:c.4367+4129_4367+4136dup | ENSP00000483745.1:n.4367+4129_4367+4136dup | |
| ENST00000617051.4:c.4489_4496dup | ENSP00000484703.1:p.Glu1500IlefsTer11 | |
| ENST00000617271.4:c.4373+1872_4373+1879dup | ENSP00000478076.1:n.4373+1872_4373+1879dup | |
| ENST00000618301.4:c.593+4129_593+4136dup | ENSP00000482780.1:n.593+4129_593+4136dup | |
| ENST00000621708.4:c.4388+1872_4388+1879dup | ENSP00000484454.1:n.4388+1872_4388+1879dup | |
| ENST00000622048.4:c.4261_4268dup | ENSP00000482329.1:p.Glu1424IlefsTer11 | |
| NM_001142763.1:c.4483_4490dup | NP_001136235.1:p.Glu1498IlefsTer11 | |
| NM_001142764.1:c.4468_4475dup | NP_001136236.1:p.Glu1493IlefsTer11 | |
| NM_001142765.1:c.4255_4262dup | NP_001136237.1:p.Glu1422IlefsTer11 | |
| NM_001142766.1:c.4453_4460dup | NP_001136238.1:p.Glu1488IlefsTer11 | |
| NM_001142767.1:c.4342_4349dup | NP_001136239.1:p.Glu1451IlefsTer11 | |
| NM_001142768.1:c.4402_4409dup | NP_001136240.1:p.Glu1471IlefsTer11 | |
| NM_001142769.1:c.4409+1872_4409+1879dup | NP_001136241.1:n.4409+1872_4409+1879dup | |
| NM_001142770.1:c.4373+1872_4373+1879dup | NP_001136242.1:n.4373+1872_4373+1879dup | |
| NM_001142771.1:c.4388+1872_4388+1879dup | NP_001136243.1:n.4388+1872_4388+1879dup | |
| NM_001142772.1:c.4373+1872_4373+1879dup | NP_001136244.1:n.4373+1872_4373+1879dup | |
| NM_001142773.1:c.4393_4400dup | NP_001136245.1:p.Glu1468IlefsTer11 | |
| NM_033056.3:c.4462_4469dup | NP_149045.3:p.Glu1491IlefsTer11 | |
| NM_001142769.2:c.4409+1872_4409+1879dup | NP_001136241.1:n.4409+1872_4409+1879dup | |
| NM_001142770.2:c.4373+1872_4373+1879dup | NP_001136242.1:n.4373+1872_4373+1879dup | |
| NM_001354404.1:c.4396_4403dup | NP_001341333.1:p.Glu1469IlefsTer11 | |
| NM_001354411.1:c.4388+4129_4388+4136dup | NP_001341340.1:n.4388+4129_4388+4136dup | |
| NM_001354420.1:c.4367+4129_4367+4136dup | NP_001341349.1:n.4367+4129_4367+4136dup | |
| NM_001354429.1:c.4367+4129_4367+4136dup | NP_001341358.1:n.4367+4129_4367+4136dup | |
| XM_017016573.2:c.4388+1872_4388+1879dup | XP_016872062.1:n.4388+1872_4388+1879dup | |
| XR_001747192.2:n.5475_5482dup | ||
| XR_001747193.2:n.5466_5473dup | ||
| NM_001142763.2:c.4483_4490dup | NP_001136235.1:p.Glu1498IlefsTer11 | |
| NM_001142764.2:c.4468_4475dup | NP_001136236.1:p.Glu1493IlefsTer11 | |
| NM_001142765.2:c.4255_4262dup | NP_001136237.1:p.Glu1422IlefsTer11 | |
| NM_001142766.2:c.4453_4460dup | NP_001136238.1:p.Glu1488IlefsTer11 | |
| NM_001142768.2:c.4402_4409dup | NP_001136240.1:p.Glu1471IlefsTer11 | |
| NM_001142769.3:c.4409+1872_4409+1879dup | NP_001136241.1:n.4409+1872_4409+1879dup | |
| NM_001142770.3:c.4373+1872_4373+1879dup | NP_001136242.1:n.4373+1872_4373+1879dup | |
| NM_001142771.2:c.4388+1872_4388+1879dup | NP_001136243.1:n.4388+1872_4388+1879dup | |
| NM_001142772.2:c.4373+1872_4373+1879dup | NP_001136244.1:n.4373+1872_4373+1879dup | |
| NM_001142773.2:c.4393_4400dup | NP_001136245.1:p.Glu1468IlefsTer11 | |
| NM_001354411.2:c.4388+4129_4388+4136dup | NP_001341340.1:n.4388+4129_4388+4136dup | |
| NM_001354420.2:c.4367+4129_4367+4136dup | NP_001341349.1:n.4367+4129_4367+4136dup | |
| NM_001354429.2:c.4367+4129_4367+4136dup | NP_001341358.1:n.4367+4129_4367+4136dup | |
| NM_033056.4:c.4462_4469dup MANE Plus Clinical | NP_149045.3:p.Glu1491IlefsTer11 | |
| NM_001142767.2:c.4342_4349dup | NP_001136239.1:p.Glu1451IlefsTer11 | |
| NM_001354404.2:c.4396_4403dup | NP_001341333.1:p.Glu1469IlefsTer11 | |
| NM_001384140.1:c.4368-3034_4368-3027dup MANE Select | NP_001371069.1:n.4368-3034_4368-3027dup |