Linked Data
dbSNP Id:
rs879131157
MyVariant Identifiers:
chr11:g.67352712_67352713insGAG (hg19)
chr11:g.67585241_67585242insGAG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67585242_67585243insAGG , CM000673.2:g.67585242_67585243insAGG | GRCh38 |
| NC_000011.9:g.67352713_67352714insAGG , CM000673.1:g.67352713_67352714insAGG | GRCh37 |
| NC_000011.8:g.67109289_67109290insAGG | NCBI36 |
| NG_012075.1:g.6648_6649insAGG , LRG_723:g.6648_6649insAGG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.336+1_336+2insAGG | ENSP00000381604.1:n.336+1_336+2insAGG | |
| ENST00000398606.10:c.336+1_336+2insAGG MANE Select | ENSP00000381607.3:n.336+1_336+2insAGG | |
| ENST00000646888.1:c.*52+1_*52+2insAGG | ENSP00000494477.1:n.*52+1_*52+2insAGG | |
| ENST00000398603.5:c.336+1_336+2insAGG | ENSP00000381604.1:n.336+1_336+2insAGG | |
| ENST00000398606.7:c.336+1_336+2insAGG | ENSP00000381607.3:n.336+1_336+2insAGG | |
| ENST00000467591.1:n.447+1_447+2insAGG | ||
| ENST00000494593.1:n.1131+1_1131+2insAGG | ||
| ENST00000498765.5:c.399+1_399+2insAGG | ||
| NM_000852.3:c.336+1_336+2insAGG , LRG_723t1:c.336+1_336+2insAGG | NP_000843.1:n.336+1_336+2insAGG | |
| NM_000852.4:c.336+1_336+2insAGG MANE Select | NP_000843.1:n.336+1_336+2insAGG |