Linked Data
ClinVar Variation Id:
55021
dbSNP Id:
rs273900717
MyVariant Identifiers:
chr17:g.41243705_41243709delinsGCCT (hg19)
chr17:g.43091688_43091692delinsGCCT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43091688_43091692delinsGCCT , CM000679.2:g.43091688_43091692delinsGCCT | GRCh38 |
| NC_000017.10:g.41243705_41243709delinsGCCT , CM000679.1:g.41243705_41243709delinsGCCT | GRCh37 |
| NC_000017.9:g.38497231_38497235delinsGCCT | NCBI36 |
| NG_005905.2:g.126292_126296delinsAGGC , LRG_292:g.126292_126296delinsAGGC |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000354071.8:n.3903_3907delinsAGGC | ||
| ENST00000461574.2:c.3839_3843delinsAGGC | ENSP00000417241.2:p.Ser1280Ter | |
| ENST00000470026.6:c.3839_3843delinsAGGC | ENSP00000419274.2:p.Ser1280Ter | |
| ENST00000473961.6:c.3713_3717delinsAGGC | ENSP00000420201.2:p.Ser1238Ter | |
| ENST00000476777.6:c.3836_3840delinsAGGC | ENSP00000417554.2:p.Ser1279Ter | |
| ENST00000477152.6:c.3761_3765delinsAGGC | ENSP00000419988.2:p.Ser1254Ter | |
| ENST00000478531.6:c.785-660_785-656delinsAGGC | ENSP00000420412.2:n.785-660_785-656delins... | |
| ENST00000489037.2:c.3761_3765delinsAGGC | ENSP00000420781.2:p.Ser1254Ter | |
| ENST00000493919.6:c.647-660_647-656delinsAGGC | ENSP00000418819.2:n.647-660_647-656delins... | |
| ENST00000494123.6:c.3839_3843delinsAGGC | ENSP00000419103.2:p.Ser1280Ter | |
| ENST00000497488.2:c.2951_2955delinsAGGC | ENSP00000418986.2:p.Ser984Ter | |
| ENST00000618469.2:c.3839_3843delinsAGGC | ENSP00000478114.2:p.Ser1280Ter | |
| ENST00000634433.2:c.3716_3720delinsAGGC | ENSP00000489431.2:p.Ser1239Ter | |
| ENST00000644379.2:c.3839_3843delinsAGGC | ENSP00000496570.2:p.Ser1280Ter | |
| ENST00000644555.2:c.647-660_647-656delinsAGGC | ENSP00000494614.2:n.647-660_647-656delins... | |
| ENST00000652672.2:c.3698_3702delinsAGGC | ENSP00000498906.2:p.Ser1233Ter | |
| ENST00000484087.6:c.665-660_665-656delinsAGGC | ENSP00000419481.2:n.665-660_665-656delins... | |
| ENST00000700182.1:c.707-660_707-656delinsAGGC | ENSP00000514849.1:n.707-660_707-656delins... | |
| ENST00000357654.9:c.3839_3843delinsAGGC MANE Select | ENSP00000350283.3:p.Ser1280Ter | |
| ENST00000471181.7:c.3839_3843delinsAGGC | ENSP00000418960.2:p.Ser1280Ter | |
| ENST00000644379.1:c.160_164delinsAGGC | ||
| ENST00000352993.7:c.671-660_671-656delinsAGGC | ENSP00000312236.5:n.671-660_671-656delins... | |
| ENST00000354071.7:c.3839_3843delinsAGGC | ENSP00000326002.7:p.Ser1280Ter | |
| ENST00000357654.7:c.3839_3843delinsAGGC | ENSP00000350283.3:p.Ser1280Ter | |
| ENST00000461221.5:c.*3622_*3626delinsAGGC | ENSP00000418548.1:n.*3622_*3626delinsAGGC... | |
| ENST00000461574.1:c.133_137delinsAGGC | ||
| ENST00000468300.5:c.788-660_788-656delinsAGGC | ENSP00000417148.1:n.788-660_788-656delins... | |
| ENST00000471181.6:c.3839_3843delinsAGGC | ENSP00000418960.2:p.Ser1280Ter | |
| ENST00000478531.5:c.785-660_785-656delinsAGGC | ENSP00000420412.1:n.785-660_785-656delins... | |
| ENST00000484087.5:c.410-660_410-656delinsAGGC | ENSP00000419481.1:n.410-660_410-656delins... | |
| ENST00000487825.5:c.413-660_413-656delinsAGGC | ENSP00000418212.1:n.413-660_413-656delins... | |
| ENST00000491747.6:c.788-660_788-656delinsAGGC | ENSP00000420705.2:n.788-660_788-656delins... | |
| ENST00000493795.5:c.3698_3702delinsAGGC | ENSP00000418775.1:p.Ser1233Ter | |
| ENST00000493919.5:c.647-660_647-656delinsAGGC | ENSP00000418819.1:n.647-660_647-656delins... | |
| ENST00000586385.5:c.5-27741_5-27737delinsAGGC | ENSP00000465818.1:n.5-27741_5-27737delins... | |
| ENST00000591534.5:c.-43-17171_-43-17167delinsAGGC | ENSP00000467329.1:n.-43-17171_-43-17167de... | |
| ENST00000591849.5:c.-99+33579_-99+33583delinsAGGC | ENSP00000465347.1:n.-99+33579_-99+33583de... | |
| NM_007294.3:c.3839_3843delinsAGGC , LRG_292t1:c.3839_3843delinsAGGC | NP_009225.1:p.Ser1280Ter | |
| NM_007297.3:c.3698_3702delinsAGGC | NP_009228.2:p.Ser1233Ter | |
| NM_007298.3:c.788-660_788-656delinsAGGC | NP_009229.2:n.788-660_788-656delinsAGGC | |
| NM_007299.3:c.788-660_788-656delinsAGGC | NP_009230.2:n.788-660_788-656delinsAGGC | |
| NM_007300.3:c.3839_3843delinsAGGC | NP_009231.2:p.Ser1280Ter | |
| NR_027676.1:n.3975_3979delinsAGGC | ||
| NM_007294.4:c.3839_3843delinsAGGC MANE Select | NP_009225.1:p.Ser1280Ter | |
| NM_007297.4:c.3698_3702delinsAGGC | NP_009228.2:p.Ser1233Ter | |
| NM_007299.4:c.788-660_788-656delinsAGGC | NP_009230.2:n.788-660_788-656delinsAGGC | |
| NM_007300.4:c.3839_3843delinsAGGC | NP_009231.2:p.Ser1280Ter | |
| NR_027676.2:n.4016_4020delinsAGGC |