Linked Data
ClinVar Variation Id:
125547
dbSNP Id:
rs80357930
ExAC:
17:41245332 T / TAG
gnomAD v2:
17-41245332-T-TAG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43093315_43093316insAG , CM000679.2:g.43093315_43093316insAG | GRCh38 |
| NC_000017.10:g.41245332_41245333insAG , CM000679.1:g.41245332_41245333insAG | GRCh37 |
| NC_000017.9:g.38498858_38498859insAG | NCBI36 |
| NG_005905.2:g.124668_124669insCT , LRG_292:g.124668_124669insCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354071.8:n.2279_2280insCT | ||
| ENST00000461574.2:c.2215_2216insCT | ENSP00000417241.2:p.Lys739ThrfsTer15 | |
| ENST00000470026.6:c.2215_2216insCT | ENSP00000419274.2:p.Lys739ThrfsTer15 | |
| ENST00000473961.6:c.2089_2090insCT | ENSP00000420201.2:p.Lys697ThrfsTer15 | |
| ENST00000476777.6:c.2212_2213insCT | ENSP00000417554.2:p.Lys738ThrfsTer15 | |
| ENST00000477152.6:c.2137_2138insCT | ENSP00000419988.2:p.Lys713ThrfsTer15 | |
| ENST00000478531.6:c.784+1428_784+1429insCT | ENSP00000420412.2:n.784+1428_784+1429insCT | |
| ENST00000489037.2:c.2137_2138insCT | ENSP00000420781.2:p.Lys713ThrfsTer15 | |
| ENST00000493919.6:c.646+1428_646+1429insCT | ENSP00000418819.2:n.646+1428_646+1429insCT | |
| ENST00000494123.6:c.2215_2216insCT | ENSP00000419103.2:p.Lys739ThrfsTer15 | |
| ENST00000497488.2:c.1327_1328insCT | ENSP00000418986.2:p.Lys443ThrfsTer15 | |
| ENST00000618469.2:c.2215_2216insCT | ENSP00000478114.2:p.Lys739ThrfsTer15 | |
| ENST00000634433.2:c.2092_2093insCT | ENSP00000489431.2:p.Lys698ThrfsTer15 | |
| ENST00000644379.2:c.2215_2216insCT | ENSP00000496570.2:p.Lys739ThrfsTer15 | |
| ENST00000644555.2:c.646+1428_646+1429insCT | ENSP00000494614.2:n.646+1428_646+1429insCT | |
| ENST00000652672.2:c.2074_2075insCT | ENSP00000498906.2:p.Lys692ThrfsTer15 | |
| ENST00000484087.6:c.664+1428_664+1429insCT | ENSP00000419481.2:n.664+1428_664+1429insCT | |
| ENST00000700182.1:c.706+1428_706+1429insCT | ENSP00000514849.1:n.706+1428_706+1429insCT | |
| ENST00000357654.9:c.2215_2216insCT MANE Select | ENSP00000350283.3:p.Lys739ThrfsTer15 | |
| ENST00000471181.7:c.2215_2216insCT | ENSP00000418960.2:p.Lys739ThrfsTer15 | |
| ENST00000352993.7:c.671-2284_671-2283insCT | ENSP00000312236.5:n.671-2284_671-2283insCT | |
| ENST00000354071.7:c.2215_2216insCT | ENSP00000326002.7:p.Lys739ThrfsTer15 | |
| ENST00000357654.7:c.2215_2216insCT | ENSP00000350283.3:p.Lys739ThrfsTer15 | |
| ENST00000461221.5:c.*1998_*1999insCT | ENSP00000418548.1:n.*1998_*1999insCT | |
| ENST00000468300.5:c.787+1428_787+1429insCT | ENSP00000417148.1:n.787+1428_787+1429insCT | |
| ENST00000471181.6:c.2215_2216insCT | ENSP00000418960.2:p.Lys739ThrfsTer15 | |
| ENST00000478531.5:c.784+1428_784+1429insCT | ENSP00000420412.1:n.784+1428_784+1429insCT | |
| ENST00000484087.5:c.409+1428_409+1429insCT | ENSP00000419481.1:n.409+1428_409+1429insCT | |
| ENST00000487825.5:c.412+1428_412+1429insCT | ENSP00000418212.1:n.412+1428_412+1429insCT | |
| ENST00000491747.6:c.787+1428_787+1429insCT | ENSP00000420705.2:n.787+1428_787+1429insCT | |
| ENST00000493795.5:c.2074_2075insCT | ENSP00000418775.1:p.Lys692ThrfsTer15 | |
| ENST00000493919.5:c.646+1428_646+1429insCT | ENSP00000418819.1:n.646+1428_646+1429insCT | |
| ENST00000586385.5:c.5-29365_5-29364insCT | ENSP00000465818.1:n.5-29365_5-29364insCT | |
| ENST00000591534.5:c.-43-18795_-43-18794insCT | ENSP00000467329.1:n.-43-18795_-43-18794insCT | |
| ENST00000591849.5:c.-99+31955_-99+31956insCT | ENSP00000465347.1:n.-99+31955_-99+31956insCT | |
| ENST00000634433.1:c.2092_2093insCT | ENSP00000489431.1:p.Lys698ThrfsTer15 | |
| NM_007294.3:c.2215_2216insCT , LRG_292t1:c.2215_2216insCT | NP_009225.1:p.Lys739ThrfsTer15 | |
| NM_007297.3:c.2074_2075insCT | NP_009228.2:p.Lys692ThrfsTer15 | |
| NM_007298.3:c.787+1428_787+1429insCT | NP_009229.2:n.787+1428_787+1429insCT | |
| NM_007299.3:c.787+1428_787+1429insCT | NP_009230.2:n.787+1428_787+1429insCT | |
| NM_007300.3:c.2215_2216insCT | NP_009231.2:p.Lys739ThrfsTer15 | |
| NR_027676.1:n.2351_2352insCT | ||
| NM_007294.4:c.2215_2216insCT MANE Select | NP_009225.1:p.Lys739ThrfsTer15 | |
| NM_007297.4:c.2074_2075insCT | NP_009228.2:p.Lys692ThrfsTer15 | |
| NM_007299.4:c.787+1428_787+1429insCT | NP_009230.2:n.787+1428_787+1429insCT | |
| NM_007300.4:c.2215_2216insCT | NP_009231.2:p.Lys739ThrfsTer15 | |
| NR_027676.2:n.2392_2393insCT |