Linked Data
ClinVar Variation Id:
164886
ClinVar RCV Id:
RCV000151619
dbSNP Id:
rs730880019
ExAC:
10:55568709 TTTC / T
gnomAD v2:
10-55568709-TTTC-T
gnomAD v3:
10-53808949-TTTC-T
gnomAD v4:
10-53808949-TTTC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.53808960_53808962del , CM000672.2:g.53808960_53808962del | GRCh38 |
| NC_000010.10:g.55568720_55568722del , CM000672.1:g.55568720_55568722del | GRCh37 |
| NC_000010.9:g.55238726_55238728del | NCBI36 |
| NG_009191.2:g.997340_997342del | |
| NG_009191.3:g.1825231_1825233del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613657.6:c.5113_5115del | ENSP00000482794.1:p.Glu1705del | |
| ENST00000395445.6:c.5092_5094del | ENSP00000378832.2:p.Glu1698del | |
| ENST00000613657.5:c.5113_5115del | ENSP00000482794.1:p.Glu1705del | |
| ENST00000642496.1:c.3530+1604_3530+1606del | ||
| ENST00000644397.2:c.4671+1604_4671+1606del MANE Select | ENSP00000495195.1:n.4671+1604_4671+1606del | |
| ENST00000373965.6:c.4482+1604_4482+1606del | ENSP00000363076.3:n.4482+1604_4482+1606del | |
| ENST00000395438.5:c.*528_*530del | ENSP00000378826.2:n.*528_*530del | |
| ENST00000395440.5:c.1900_1902del | ENSP00000378827.1:p.Glu634del | |
| ENST00000395442.5:c.1693_1695del | ENSP00000378829.1:p.Glu565del | |
| ENST00000395445.5:c.5092_5094del | ENSP00000378832.2:p.Glu1698del | |
| ENST00000395446.5:c.2686_2688del | ENSP00000378833.1:p.Glu896del | |
| ENST00000409834.5:c.*528_*530del | ENSP00000386693.1:n.*528_*530del | |
| ENST00000414367.5:c.*1151_*1153del | ENSP00000412531.1:n.*1151_*1153del | |
| ENST00000414778.5:c.4479+1604_4479+1606del | ENSP00000410304.2:n.4479+1604_4479+1606del | |
| ENST00000476074.5:n.609+1604_609+1606del | ||
| ENST00000495484.5:c.699+1604_699+1606del | ENSP00000480780.1:n.699+1604_699+1606del | |
| ENST00000612394.4:c.5110_5112del | ENSP00000482921.1:p.Glu1704del | |
| ENST00000613657.4:c.5113_5115del | ENSP00000482794.1:p.Glu1705del | |
| ENST00000614895.4:c.4494+1604_4494+1606del | ENSP00000478512.1:n.4494+1604_4494+1606del | |
| ENST00000615043.1:c.713_715del | ||
| ENST00000616114.4:c.4476+1604_4476+1606del | ENSP00000483745.1:n.4476+1604_4476+1606del | |
| ENST00000617271.4:c.*528_*530del | ENSP00000478076.1:n.*528_*530del | |
| ENST00000618301.4:c.831+1604_831+1606del | ENSP00000482780.1:n.831+1604_831+1606del | |
| ENST00000621708.4:c.4497+1604_4497+1606del | ENSP00000484454.1:n.4497+1604_4497+1606del | |
| NM_001142769.1:c.5113_5115del | NP_001136241.1:p.Glu1705del | |
| NM_001142770.1:c.*528_*530del | NP_001136242.1:n.*528_*530del | |
| NM_001142771.1:c.4497+1604_4497+1606del | NP_001136243.1:n.4497+1604_4497+1606del | |
| NM_001142772.1:c.4482+1604_4482+1606del | NP_001136244.1:n.4482+1604_4482+1606del | |
| NM_001142769.2:c.5113_5115del | NP_001136241.1:p.Glu1705del | |
| NM_001142770.2:c.*528_*530del | NP_001136242.1:n.*528_*530del | |
| NM_001354411.1:c.5092_5094del | NP_001341340.1:p.Glu1698del | |
| NM_001354420.1:c.4476+1604_4476+1606del | NP_001341349.1:n.4476+1604_4476+1606del | |
| NM_001354429.1:c.4605+1604_4605+1606del | NP_001341358.1:n.4605+1604_4605+1606del | |
| XM_017016573.2:c.5092_5094del | XP_016872062.1:p.Glu1698del | |
| XR_001747192.2:n.10963+1604_10963+1606del | ||
| XR_001747193.2:n.10954+1604_10954+1606del | ||
| NM_001142769.3:c.5113_5115del | NP_001136241.1:p.Glu1705del | |
| NM_001142770.3:c.*528_*530del | NP_001136242.1:n.*528_*530del | |
| NM_001142771.2:c.4497+1604_4497+1606del | NP_001136243.1:n.4497+1604_4497+1606del | |
| NM_001142772.2:c.4482+1604_4482+1606del | NP_001136244.1:n.4482+1604_4482+1606del | |
| NM_001354411.2:c.5092_5094del | NP_001341340.1:p.Glu1698del | |
| NM_001354420.2:c.4476+1604_4476+1606del | NP_001341349.1:n.4476+1604_4476+1606del | |
| NM_001354429.2:c.4605+1604_4605+1606del | NP_001341358.1:n.4605+1604_4605+1606del | |
| NM_001384140.1:c.4671+1604_4671+1606del MANE Select | NP_001371069.1:n.4671+1604_4671+1606del |