Linked Data
ClinVar Variation Id:
54521
ClinVar RCV Id:
RCV000111816
dbSNP Id:
rs80357657
PubMed:
PMID:8644702
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43093248_43093249del , CM000679.2:g.43093248_43093249del | GRCh38 |
| NC_000017.10:g.41245265_41245266del , CM000679.1:g.41245265_41245266del | GRCh37 |
| NC_000017.9:g.38498791_38498792del | NCBI36 |
| NG_005905.2:g.124736_124737del , LRG_292:g.124736_124737del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000354071.8:n.2347_2348del | ||
| ENST00000461574.2:c.2283_2284del | ENSP00000417241.2:p.Arg762IlefsTer5 | |
| ENST00000470026.6:c.2283_2284del | ENSP00000419274.2:p.Arg762IlefsTer5 | |
| ENST00000473961.6:c.2157_2158del | ENSP00000420201.2:p.Arg720IlefsTer5 | |
| ENST00000476777.6:c.2280_2281del | ENSP00000417554.2:p.Arg761IlefsTer5 | |
| ENST00000477152.6:c.2205_2206del | ENSP00000419988.2:p.Arg736IlefsTer5 | |
| ENST00000478531.6:c.784+1496_784+1497del | ENSP00000420412.2:n.784+1496_784+1497del | |
| ENST00000489037.2:c.2205_2206del | ENSP00000420781.2:p.Arg736IlefsTer5 | |
| ENST00000493919.6:c.646+1496_646+1497del | ENSP00000418819.2:n.646+1496_646+1497del | |
| ENST00000494123.6:c.2283_2284del | ENSP00000419103.2:p.Arg762IlefsTer5 | |
| ENST00000497488.2:c.1395_1396del | ENSP00000418986.2:p.Arg466IlefsTer5 | |
| ENST00000618469.2:c.2283_2284del | ENSP00000478114.2:p.Arg762IlefsTer5 | |
| ENST00000634433.2:c.2160_2161del | ENSP00000489431.2:p.Arg721IlefsTer5 | |
| ENST00000644379.2:c.2283_2284del | ENSP00000496570.2:p.Arg762IlefsTer5 | |
| ENST00000644555.2:c.646+1496_646+1497del | ENSP00000494614.2:n.646+1496_646+1497del | |
| ENST00000652672.2:c.2142_2143del | ENSP00000498906.2:p.Arg715IlefsTer5 | |
| ENST00000484087.6:c.664+1496_664+1497del | ENSP00000419481.2:n.664+1496_664+1497del | |
| ENST00000700182.1:c.706+1496_706+1497del | ENSP00000514849.1:n.706+1496_706+1497del | |
| ENST00000357654.9:c.2283_2284del MANE Select | ENSP00000350283.3:p.Arg762IlefsTer5 | |
| ENST00000471181.7:c.2283_2284del | ENSP00000418960.2:p.Arg762IlefsTer5 | |
| ENST00000352993.7:c.671-2216_671-2215del | ENSP00000312236.5:n.671-2216_671-2215del | |
| ENST00000354071.7:c.2283_2284del | ENSP00000326002.7:p.Arg762IlefsTer5 | |
| ENST00000357654.7:c.2283_2284del | ENSP00000350283.3:p.Arg762IlefsTer5 | |
| ENST00000461221.5:c.*2066_*2067del | ENSP00000418548.1:n.*2066_*2067del | |
| ENST00000468300.5:c.787+1496_787+1497del | ENSP00000417148.1:n.787+1496_787+1497del | |
| ENST00000471181.6:c.2283_2284del | ENSP00000418960.2:p.Arg762IlefsTer5 | |
| ENST00000478531.5:c.784+1496_784+1497del | ENSP00000420412.1:n.784+1496_784+1497del | |
| ENST00000484087.5:c.409+1496_409+1497del | ENSP00000419481.1:n.409+1496_409+1497del | |
| ENST00000487825.5:c.412+1496_412+1497del | ENSP00000418212.1:n.412+1496_412+1497del | |
| ENST00000491747.6:c.787+1496_787+1497del | ENSP00000420705.2:n.787+1496_787+1497del | |
| ENST00000493795.5:c.2142_2143del | ENSP00000418775.1:p.Arg715IlefsTer5 | |
| ENST00000493919.5:c.646+1496_646+1497del | ENSP00000418819.1:n.646+1496_646+1497del | |
| ENST00000586385.5:c.5-29297_5-29296del | ENSP00000465818.1:n.5-29297_5-29296del | |
| ENST00000591534.5:c.-43-18727_-43-18726del | ENSP00000467329.1:n.-43-18727_-43-18726de... | |
| ENST00000591849.5:c.-99+32023_-99+32024del | ENSP00000465347.1:n.-99+32023_-99+32024de... | |
| ENST00000634433.1:c.2160_2161del | ENSP00000489431.1:p.Arg721IlefsTer5 | |
| NM_007294.3:c.2283_2284del , LRG_292t1:c.2283_2284del | NP_009225.1:p.Arg762IlefsTer5 | |
| NM_007297.3:c.2142_2143del | NP_009228.2:p.Arg715IlefsTer5 | |
| NM_007298.3:c.787+1496_787+1497del | NP_009229.2:n.787+1496_787+1497del | |
| NM_007299.3:c.787+1496_787+1497del | NP_009230.2:n.787+1496_787+1497del | |
| NM_007300.3:c.2283_2284del | NP_009231.2:p.Arg762IlefsTer5 | |
| NR_027676.1:n.2419_2420del | ||
| NM_007294.4:c.2283_2284del MANE Select | NP_009225.1:p.Arg762IlefsTer5 | |
| NM_007297.4:c.2142_2143del | NP_009228.2:p.Arg715IlefsTer5 | |
| NM_007299.4:c.787+1496_787+1497del | NP_009230.2:n.787+1496_787+1497del | |
| NM_007300.4:c.2283_2284del | NP_009231.2:p.Arg762IlefsTer5 | |
| NR_027676.2:n.2460_2461del |