Linked Data
ClinVar Variation Id:
53696
ClinVar RCV Id:
RCV003474573
dbSNP Id:
rs121908798
MyVariant Identifiers:
chr7:g.117171004_117171006delinsG (hg19)
chr7:g.117530950_117530952delinsG (hg38)
PubMed:
PMID:23974870
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117530950_117530952delinsG , CM000669.2:g.117530950_117530952delinsG | GRCh38 |
| NC_000007.13:g.117171004_117171006delinsG , CM000669.1:g.117171004_117171006delinsG | GRCh37 |
| NC_000007.12:g.116958240_116958242delinsG | NCBI36 |
| NG_016465.4:g.70167_70169delinsG , LRG_663:g.70167_70169delinsG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647720.2:c.325_327delinsG | ENSP00000497673.2:p.Tyr109GlyfsTer4 | |
| ENST00000647978.2:c.*222_*224delinsG | ENSP00000497658.1:n.*222_*224delinsG | |
| ENST00000649781.2:c.325_327delinsG | ENSP00000497203.1:p.Tyr109GlyfsTer4 | |
| ENST00000685018.2:c.325_327delinsG | ENSP00000510194.2:p.Tyr109GlyfsTer4 | |
| ENST00000687278.2:c.325_327delinsG | ENSP00000509593.2:p.Tyr109GlyfsTer4 | |
| ENST00000699585.1:c.325_327delinsG | ENSP00000514456.1:p.Tyr109GlyfsTer4 | |
| ENST00000699596.1:c.325_327delinsG | ENSP00000514465.1:p.Tyr109GlyfsTer4 | |
| ENST00000699597.1:c.325_327delinsG | ENSP00000514466.1:p.Tyr109GlyfsTer4 | |
| ENST00000699598.1:c.325_327delinsG | ENSP00000514467.1:p.Tyr109GlyfsTer4 | |
| ENST00000699599.1:c.325_327delinsG | ENSP00000514468.1:p.Tyr109GlyfsTer4 | |
| ENST00000699600.1:c.325_327delinsG | ENSP00000514469.1:p.Tyr109GlyfsTer4 | |
| ENST00000699601.1:c.325_327delinsG | ENSP00000514470.1:p.Tyr109GlyfsTer4 | |
| ENST00000699602.1:c.325_327delinsG | ENSP00000514471.1:p.Tyr109GlyfsTer4 | |
| ENST00000699604.1:c.*149_*151delinsG | ENSP00000514472.1:n.*149_*151delinsG | |
| ENST00000699605.1:c.82_84delinsG | ENSP00000514473.1:p.Tyr28GlyfsTer4 | |
| ENST00000446805.2:c.82_84delinsG | ENSP00000417012.1:p.Tyr28GlyfsTer4 | |
| ENST00000003084.11:c.325_327delinsG MANE Select | ENSP00000003084.6:p.Tyr109GlyfsTer4 | |
| ENST00000647978.1:c.*222_*224delinsG | ENSP00000497658.1:n.*222_*224delinsG | |
| ENST00000648260.1:c.325_327delinsG | ENSP00000497957.1:p.Tyr109GlyfsTer4 | |
| ENST00000649406.1:c.325_327delinsG | ENSP00000497965.1:p.Tyr109GlyfsTer4 | |
| ENST00000649781.1:c.325_327delinsG | ENSP00000497203.1:p.Tyr109GlyfsTer4 | |
| ENST00000673785.1:c.82_84delinsG | ENSP00000501235.1:p.Tyr28GlyfsTer4 | |
| ENST00000003084.10:c.325_327delinsG | ENSP00000003084.6:p.Tyr109GlyfsTer4 | |
| ENST00000426809.5:c.325_327delinsG | ENSP00000389119.1:p.Tyr109GlyfsTer4 | |
| ENST00000446805.1:c.82_84delinsG | ENSP00000417012.1:p.Tyr28GlyfsTer4 | |
| NM_000492.3:c.325_327delinsG , LRG_663t1:c.325_327delinsG | NP_000483.3:p.Tyr109GlyfsTer4 | |
| XM_011515751.1:c.415_417delinsG | XP_011514053.1:p.Tyr139GlyfsTer4 | |
| XM_011515752.1:c.415_417delinsG | XP_011514054.1:p.Tyr139GlyfsTer4 | |
| XM_011515753.1:c.82_84delinsG | XP_011514055.1:p.Tyr28GlyfsTer4 | |
| XM_011515754.1:c.82_84delinsG | XP_011514056.1:p.Tyr28GlyfsTer4 | |
| NM_000492.4:c.325_327delinsG MANE Select | NP_000483.3:p.Tyr109GlyfsTer4 |