Linked Data
ClinVar Variation Id:
125609
ClinVar RCV Id:
RCV000112011
dbSNP Id:
rs80357769
PubMed:
PMID:23536787
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43092372_43092373insC , CM000679.2:g.43092372_43092373insC | GRCh38 |
| NC_000017.10:g.41244389_41244390insC , CM000679.1:g.41244389_41244390insC | GRCh37 |
| NC_000017.9:g.38497915_38497916insC | NCBI36 |
| NG_005905.2:g.125611_125612insG , LRG_292:g.125611_125612insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354071.8:n.3222_3223insG | ||
| ENST00000461574.2:c.3158_3159insG | ENSP00000417241.2:p.Val1054SerfsTer6 | |
| ENST00000470026.6:c.3158_3159insG | ENSP00000419274.2:p.Val1054SerfsTer6 | |
| ENST00000473961.6:c.3032_3033insG | ENSP00000420201.2:p.Val1012SerfsTer6 | |
| ENST00000476777.6:c.3155_3156insG | ENSP00000417554.2:p.Val1053SerfsTer6 | |
| ENST00000477152.6:c.3080_3081insG | ENSP00000419988.2:p.Val1028SerfsTer6 | |
| ENST00000478531.6:c.785-1341_785-1340insG | ENSP00000420412.2:n.785-1341_785-1340insG | |
| ENST00000489037.2:c.3080_3081insG | ENSP00000420781.2:p.Val1028SerfsTer6 | |
| ENST00000493919.6:c.647-1341_647-1340insG | ENSP00000418819.2:n.647-1341_647-1340insG | |
| ENST00000494123.6:c.3158_3159insG | ENSP00000419103.2:p.Val1054SerfsTer6 | |
| ENST00000497488.2:c.2270_2271insG | ENSP00000418986.2:p.Val758SerfsTer6 | |
| ENST00000618469.2:c.3158_3159insG | ENSP00000478114.2:p.Val1054SerfsTer6 | |
| ENST00000634433.2:c.3035_3036insG | ENSP00000489431.2:p.Val1013SerfsTer6 | |
| ENST00000644379.2:c.3158_3159insG | ENSP00000496570.2:p.Val1054SerfsTer6 | |
| ENST00000644555.2:c.647-1341_647-1340insG | ENSP00000494614.2:n.647-1341_647-1340insG | |
| ENST00000652672.2:c.3017_3018insG | ENSP00000498906.2:p.Val1007SerfsTer6 | |
| ENST00000484087.6:c.665-1341_665-1340insG | ENSP00000419481.2:n.665-1341_665-1340insG | |
| ENST00000700182.1:c.707-1341_707-1340insG | ENSP00000514849.1:n.707-1341_707-1340insG | |
| ENST00000357654.9:c.3158_3159insG MANE Select | ENSP00000350283.3:p.Val1054SerfsTer6 | |
| ENST00000471181.7:c.3158_3159insG | ENSP00000418960.2:p.Val1054SerfsTer6 | |
| ENST00000352993.7:c.671-1341_671-1340insG | ENSP00000312236.5:n.671-1341_671-1340insG | |
| ENST00000354071.7:c.3158_3159insG | ENSP00000326002.7:p.Val1054SerfsTer6 | |
| ENST00000357654.7:c.3158_3159insG | ENSP00000350283.3:p.Val1054SerfsTer6 | |
| ENST00000461221.5:c.*2941_*2942insG | ENSP00000418548.1:n.*2941_*2942insG | |
| ENST00000468300.5:c.788-1341_788-1340insG | ENSP00000417148.1:n.788-1341_788-1340insG | |
| ENST00000471181.6:c.3158_3159insG | ENSP00000418960.2:p.Val1054SerfsTer6 | |
| ENST00000478531.5:c.785-1341_785-1340insG | ENSP00000420412.1:n.785-1341_785-1340insG | |
| ENST00000484087.5:c.410-1341_410-1340insG | ENSP00000419481.1:n.410-1341_410-1340insG | |
| ENST00000487825.5:c.413-1341_413-1340insG | ENSP00000418212.1:n.413-1341_413-1340insG | |
| ENST00000491747.6:c.788-1341_788-1340insG | ENSP00000420705.2:n.788-1341_788-1340insG | |
| ENST00000493795.5:c.3017_3018insG | ENSP00000418775.1:p.Val1007SerfsTer6 | |
| ENST00000493919.5:c.647-1341_647-1340insG | ENSP00000418819.1:n.647-1341_647-1340insG | |
| ENST00000586385.5:c.5-28422_5-28421insG | ENSP00000465818.1:n.5-28422_5-28421insG | |
| ENST00000591534.5:c.-43-17852_-43-17851insG | ENSP00000467329.1:n.-43-17852_-43-17851insG | |
| ENST00000591849.5:c.-99+32898_-99+32899insG | ENSP00000465347.1:n.-99+32898_-99+32899insG | |
| NM_007294.3:c.3158_3159insG , LRG_292t1:c.3158_3159insG | NP_009225.1:p.Val1054SerfsTer6 | |
| NM_007297.3:c.3017_3018insG | NP_009228.2:p.Val1007SerfsTer6 | |
| NM_007298.3:c.788-1341_788-1340insG | NP_009229.2:n.788-1341_788-1340insG | |
| NM_007299.3:c.788-1341_788-1340insG | NP_009230.2:n.788-1341_788-1340insG | |
| NM_007300.3:c.3158_3159insG | NP_009231.2:p.Val1054SerfsTer6 | |
| NR_027676.1:n.3294_3295insG | ||
| NM_007294.4:c.3158_3159insG MANE Select | NP_009225.1:p.Val1054SerfsTer6 | |
| NM_007297.4:c.3017_3018insG | NP_009228.2:p.Val1007SerfsTer6 | |
| NM_007299.4:c.788-1341_788-1340insG | NP_009230.2:n.788-1341_788-1340insG | |
| NM_007300.4:c.3158_3159insG | NP_009231.2:p.Val1054SerfsTer6 | |
| NR_027676.2:n.3335_3336insG |