Linked Data
ClinVar Variation Id:
54137
ClinVar RCV Id:
RCV000111555
dbSNP Id:
rs273897652
MyVariant Identifiers:
chr17:g.41246425_41246427delinsA (hg19)
chr17:g.43094408_43094410delinsA (hg38)
PubMed:
PMID:12955716
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43094408_43094410delinsA , CM000679.2:g.43094408_43094410delinsA | GRCh38 |
| NC_000017.10:g.41246425_41246427delinsA , CM000679.1:g.41246425_41246427delinsA | GRCh37 |
| NC_000017.9:g.38499951_38499953delinsA | NCBI36 |
| NG_005905.2:g.123574_123576delinsT , LRG_292:g.123574_123576delinsT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354071.8:n.1185_1187delinsT | ||
| ENST00000461574.2:c.1121_1123delinsT | ENSP00000417241.2:p.Thr374IlefsTer3 | |
| ENST00000470026.6:c.1121_1123delinsT | ENSP00000419274.2:p.Thr374IlefsTer3 | |
| ENST00000473961.6:c.995_997delinsT | ENSP00000420201.2:p.Thr332IlefsTer3 | |
| ENST00000476777.6:c.1118_1120delinsT | ENSP00000417554.2:p.Thr373IlefsTer3 | |
| ENST00000477152.6:c.1043_1045delinsT | ENSP00000419988.2:p.Thr348IlefsTer3 | |
| ENST00000478531.6:c.784+334_784+336delinsT | ENSP00000420412.2:n.784+334_784+336delinsT | |
| ENST00000489037.2:c.1043_1045delinsT | ENSP00000420781.2:p.Thr348IlefsTer3 | |
| ENST00000493919.6:c.646+334_646+336delinsT | ENSP00000418819.2:n.646+334_646+336delinsT | |
| ENST00000494123.6:c.1121_1123delinsT | ENSP00000419103.2:p.Thr374IlefsTer3 | |
| ENST00000497488.2:c.233_235delinsT | ENSP00000418986.2:p.Thr78IlefsTer3 | |
| ENST00000618469.2:c.1121_1123delinsT | ENSP00000478114.2:p.Thr374IlefsTer3 | |
| ENST00000634433.2:c.998_1000delinsT | ENSP00000489431.2:p.Thr333IlefsTer3 | |
| ENST00000644379.2:c.1121_1123delinsT | ENSP00000496570.2:p.Thr374IlefsTer3 | |
| ENST00000644555.2:c.646+334_646+336delinsT | ENSP00000494614.2:n.646+334_646+336delinsT | |
| ENST00000652672.2:c.980_982delinsT | ENSP00000498906.2:p.Thr327IlefsTer3 | |
| ENST00000484087.6:c.664+334_664+336delinsT | ENSP00000419481.2:n.664+334_664+336delinsT | |
| ENST00000700182.1:c.706+334_706+336delinsT | ENSP00000514849.1:n.706+334_706+336delinsT | |
| ENST00000700183.1:c.*1129_*1131delinsT | ENSP00000514850.1:n.*1129_*1131delinsT | |
| ENST00000357654.9:c.1121_1123delinsT MANE Select | ENSP00000350283.3:p.Thr374IlefsTer3 | |
| ENST00000471181.7:c.1121_1123delinsT | ENSP00000418960.2:p.Thr374IlefsTer3 | |
| ENST00000652672.1:c.980_982delinsT | ENSP00000498906.1:p.Thr327IlefsTer3 | |
| ENST00000352993.7:c.670+1436_670+1438delinsT | ENSP00000312236.5:n.670+1436_670+1438delinsT | |
| ENST00000354071.7:c.1121_1123delinsT | ENSP00000326002.7:p.Thr374IlefsTer3 | |
| ENST00000357654.7:c.1121_1123delinsT | ENSP00000350283.3:p.Thr374IlefsTer3 | |
| ENST00000412061.3:c.472_474delinsT | ||
| ENST00000461221.5:c.*904_*906delinsT | ENSP00000418548.1:n.*904_*906delinsT | |
| ENST00000468300.5:c.787+334_787+336delinsT | ENSP00000417148.1:n.787+334_787+336delinsT | |
| ENST00000470026.5:c.1121_1123delinsT | ENSP00000419274.1:p.Thr374IlefsTer3 | |
| ENST00000471181.6:c.1121_1123delinsT | ENSP00000418960.2:p.Thr374IlefsTer3 | |
| ENST00000473961.5:c.718_720delinsT | ||
| ENST00000477152.5:c.1043_1045delinsT | ENSP00000419988.1:p.Thr348IlefsTer3 | |
| ENST00000478531.5:c.784+334_784+336delinsT | ENSP00000420412.1:n.784+334_784+336delinsT | |
| ENST00000484087.5:c.409+334_409+336delinsT | ENSP00000419481.1:n.409+334_409+336delinsT | |
| ENST00000487825.5:c.412+334_412+336delinsT | ENSP00000418212.1:n.412+334_412+336delinsT | |
| ENST00000491747.6:c.787+334_787+336delinsT | ENSP00000420705.2:n.787+334_787+336delinsT | |
| ENST00000492859.5:c.*1057_*1059delinsT | ENSP00000420253.1:n.*1057_*1059delinsT | |
| ENST00000493795.5:c.980_982delinsT | ENSP00000418775.1:p.Thr327IlefsTer3 | |
| ENST00000493919.5:c.646+334_646+336delinsT | ENSP00000418819.1:n.646+334_646+336delinsT | |
| ENST00000494123.5:c.1121_1123delinsT | ENSP00000419103.1:p.Thr374IlefsTer3 | |
| ENST00000497488.1:c.233_235delinsT | ENSP00000418986.1:p.Thr78IlefsTer3 | |
| ENST00000586385.5:c.5-30459_5-30457delinsT | ENSP00000465818.1:n.5-30459_5-30457delinsT | |
| ENST00000591534.5:c.-43-19889_-43-19887delinsT | ENSP00000467329.1:n.-43-19889_-43-19887delinsT | |
| ENST00000591849.5:c.-99+30861_-99+30863delinsT | ENSP00000465347.1:n.-99+30861_-99+30863delinsT | |
| ENST00000634433.1:c.998_1000delinsT | ENSP00000489431.1:p.Thr333IlefsTer3 | |
| NM_007294.3:c.1121_1123delinsT , LRG_292t1:c.1121_1123delinsT | NP_009225.1:p.Thr374IlefsTer3 | |
| NM_007297.3:c.980_982delinsT | NP_009228.2:p.Thr327IlefsTer3 | |
| NM_007298.3:c.787+334_787+336delinsT | NP_009229.2:n.787+334_787+336delinsT | |
| NM_007299.3:c.787+334_787+336delinsT | NP_009230.2:n.787+334_787+336delinsT | |
| NM_007300.3:c.1121_1123delinsT | NP_009231.2:p.Thr374IlefsTer3 | |
| NR_027676.1:n.1257_1259delinsT | ||
| NM_007294.4:c.1121_1123delinsT MANE Select | NP_009225.1:p.Thr374IlefsTer3 | |
| NM_007297.4:c.980_982delinsT | NP_009228.2:p.Thr327IlefsTer3 | |
| NM_007299.4:c.787+334_787+336delinsT | NP_009230.2:n.787+334_787+336delinsT | |
| NM_007300.4:c.1121_1123delinsT | NP_009231.2:p.Thr374IlefsTer3 | |
| NR_027676.2:n.1298_1300delinsT |