Linked Data
dbSNP Id:
rs1329970389
MyVariant Identifiers:
chr14:g.73640207_73640208insGGTGGG (hg19)
chr14:g.73173499_73173500insGGTGGG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.73173504_73173505insGGGTGG , CM000676.2:g.73173504_73173505insGGGTGG | GRCh38 |
| NC_000014.8:g.73640212_73640213insGGGTGG , CM000676.1:g.73640212_73640213insGGGTGG | GRCh37 |
| NC_000014.7:g.72709965_72709966insGGGTGG | NCBI36 |
| NG_007386.2:g.42034_42035insGGGTGG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000324501.10:c.339-62_339-61insGGGTGG MANE Select | ENSP00000326366.5:n.339-62_339-61insGGGTG... | |
| ENST00000324501.9:c.339-62_339-61insGGGTGG | ENSP00000326366.5:n.339-62_339-61insGGGTG... | |
| ENST00000357710.8:c.327-62_327-61insGGGTGG | ENSP00000350342.4:n.327-62_327-61insGGGTG... | |
| ENST00000394157.7:c.339-62_339-61insGGGTGG | ENSP00000377712.3:n.339-62_339-61insGGGTG... | |
| ENST00000394164.5:c.327-62_327-61insGGGTGG | ENSP00000377719.1:n.327-62_327-61insGGGTG... | |
| ENST00000406768.1:c.63-62_63-61insGGGTGG | ENSP00000385948.1:n.63-62_63-61insGGGTGG | |
| ENST00000553719.5:c.327-62_327-61insGGGTGG | ENSP00000451674.1:n.327-62_327-61insGGGTG... | |
| ENST00000553855.5:c.339-62_339-61insGGGTGG | ENSP00000452242.1:n.339-62_339-61insGGGTG... | |
| ENST00000555254.5:c.339-62_339-61insGGGTGG | ENSP00000450652.1:n.339-62_339-61insGGGTG... | |
| ENST00000555386.5:c.327-62_327-61insGGGTGG | ENSP00000450845.1:n.327-62_327-61insGGGTG... | |
| ENST00000557356.5:c.327-62_327-61insGGGTGG | ENSP00000451498.1:n.327-62_327-61insGGGTG... | |
| ENST00000557511.5:c.339-62_339-61insGGGTGG | ENSP00000451429.1:n.339-62_339-61insGGGTG... | |
| ENST00000559361.5:c.*283-62_*283-61insGGGTGG | ENSP00000454156.1:n.*283-62_*283-61insGGG... | |
| NM_000021.3:c.339-62_339-61insGGGTGG | NP_000012.1:n.339-62_339-61insGGGTGG | |
| NM_007318.2:c.327-62_327-61insGGGTGG | NP_015557.2:n.327-62_327-61insGGGTGG | |
| XM_005267864.1:c.339-62_339-61insGGGTGG | XP_005267921.1:n.339-62_339-61insGGGTGG | |
| XM_005267866.1:c.327-62_327-61insGGGTGG | XP_005267923.1:n.327-62_327-61insGGGTGG | |
| XM_011536971.1:c.339-62_339-61insGGGTGG | XP_011535273.1:n.339-62_339-61insGGGTGG | |
| XM_011536972.1:c.339-62_339-61insGGGTGG | XP_011535274.1:n.339-62_339-61insGGGTGG | |
| XM_011536973.1:c.327-62_327-61insGGGTGG | XP_011535275.1:n.327-62_327-61insGGGTGG | |
| XM_011536974.1:c.327-62_327-61insGGGTGG | XP_011535276.1:n.327-62_327-61insGGGTGG | |
| XM_005267864.3:c.339-62_339-61insGGGTGG | XP_005267921.1:n.339-62_339-61insGGGTGG | |
| XM_005267866.2:c.327-62_327-61insGGGTGG | XP_005267923.1:n.327-62_327-61insGGGTGG | |
| XM_011536972.2:c.339-62_339-61insGGGTGG | XP_011535274.1:n.339-62_339-61insGGGTGG | |
| XM_011536973.2:c.327-62_327-61insGGGTGG | XP_011535275.1:n.327-62_327-61insGGGTGG | |
| XM_011536974.2:c.327-62_327-61insGGGTGG | XP_011535276.1:n.327-62_327-61insGGGTGG | |
| NM_000021.4:c.339-62_339-61insGGGTGG MANE Select | NP_000012.1:n.339-62_339-61insGGGTGG | |
| NM_007318.3:c.327-62_327-61insGGGTGG | NP_015557.2:n.327-62_327-61insGGGTGG |