Linked Data
dbSNP Id:
rs1565325289
gnomAD v2:
11-116661862-G-GCCC
MyVariant Identifiers:
chr11:g.116661862_116661863insCCC (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116791146_116791147insCCC , CM000673.2:g.116791146_116791147insCCC | GRCh38 |
| NC_000011.9:g.116661862_116661863insCCC , CM000673.1:g.116661862_116661863insCCC | GRCh37 |
| NC_000011.8:g.116167072_116167073insCCC | NCBI36 |
| NG_015894.1:g.6274_6275insGGG | |
| NG_015894.2:g.6274_6275insGGG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227665.9:c.162-80_162-79insGGG MANE Select | ENSP00000227665.4:n.162-80_162-79insGGG | |
| ENST00000433069.2:c.162-80_162-79insGGG | ENSP00000399701.2:n.162-80_162-79insGGG | |
| ENST00000673688.1:c.166_167insGGG | ENSP00000501141.1:p.Ser56delinsTrpAla | |
| ENST00000227665.8:c.162-80_162-79insGGG | ENSP00000227665.4:n.162-80_162-79insGGG | |
| ENST00000433069.1:c.162-80_162-79insGGG | ENSP00000399701.1:n.162-80_162-79insGGG | |
| ENST00000542499.5:c.162-80_162-79insGGG | ENSP00000445002.1:n.162-80_162-79insGGG | |
| NM_001166598.1:c.162-80_162-79insGGG | NP_001160070.1:n.162-80_162-79insGGG | |
| NM_052968.4:c.162-80_162-79insGGG | NP_443200.2:n.162-80_162-79insGGG | |
| NM_001166598.2:c.162-80_162-79insGGG | NP_001160070.1:n.162-80_162-79insGGG | |
| NM_001371904.1:c.162-80_162-79insGGG MANE Select | NP_001358833.1:n.162-80_162-79insGGG | |
| NM_052968.5:c.162-80_162-79insGGG | NP_443200.2:n.162-80_162-79insGGG |