Linked Data
ClinVar Variation Id:
217011
ClinVar RCV Id:
RCV000196238
dbSNP Id:
rs863224929
MyVariant Identifiers:
chr6:g.152770776_152770786delinsG (hg19)
chr6:g.152449641_152449651delinsG (hg38)
PubMed:
PMID:25326637
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152449641_152449651delinsG , CM000668.2:g.152449641_152449651delinsG | GRCh38 |
| NC_000006.11:g.152770776_152770786delinsG , CM000668.1:g.152770776_152770786delinsG | GRCh37 |
| NC_000006.10:g.152812469_152812479delinsG | NCBI36 |
| NG_012855.1:g.192749_192759delinsC | |
| NG_012855.2:g.192749_192759delinsC |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000367255.10:c.3396-10_3396delinsC | ||
| ENST00000423061.6:c.3417-10_3417delinsC | ||
| ENST00000671915.1:c.693-10_693delinsC | ||
| ENST00000672122.1:c.3339-10_3339delinsC | ||
| ENST00000673163.1:c.*3366-10_*3366delinsC | ||
| ENST00000673281.1:c.3390-10_3390delinsC | ||
| ENST00000341594.9:c.3543-10_3543delinsC | ||
| ENST00000367248.7:c.3366-10_3366delinsC | ||
| ENST00000367253.8:c.3396-10_3396delinsC | ||
| ENST00000367255.9:c.3396-10_3396delinsC | ||
| ENST00000413186.6:c.3396-10_3396delinsC | ||
| ENST00000423061.5:c.3417-10_3417delinsC | ||
| ENST00000461872.6:n.3614-10_3614delinsC | ||
| NM_033071.3:c.3417-10_3417delinsC | ||
| NM_182961.3:c.3396-10_3396delinsC | ||
| XM_006715407.1:c.3417-10_3417delinsC | ||
| XM_006715408.1:c.3417-10_3417delinsC | ||
| XM_006715409.1:c.3396-10_3396delinsC | ||
| XM_006715410.1:c.3417-10_3417delinsC | ||
| XM_006715411.1:c.3366-10_3366delinsC | ||
| XM_006715412.1:c.3417-10_3417delinsC | ||
| XM_006715413.1:c.3417-10_3417delinsC | ||
| XM_006715414.1:c.3345-10_3345delinsC | ||
| XM_006715415.1:c.3417-10_3417delinsC | ||
| XM_006715416.1:c.3417-10_3417delinsC | ||
| XM_006715417.1:c.3417-10_3417delinsC | ||
| XM_006715420.1:c.3417-10_3417delinsC | ||
| XM_006715421.1:c.3417-10_3417delinsC | ||
| XM_006715422.1:c.3258-10_3258delinsC | ||
| XM_006715423.1:c.3417-10_3417delinsC | ||
| XM_006715424.1:c.3417-10_3417delinsC | ||
| XM_006715425.1:c.3417-10_3417delinsC | ||
| XM_011535641.1:c.3417-10_3417delinsC | ||
| XM_011535642.1:c.3417-10_3417delinsC | ||
| XM_011535643.1:c.3252-10_3252delinsC | ||
| XM_011535644.1:c.1692-10_1692delinsC | ||
| XM_011535645.1:c.1185-10_1185delinsC | ||
| XM_011535646.1:c.3417-10_3417delinsC | ||
| XM_006715408.2:c.3417-10_3417delinsC | ||
| XM_006715410.2:c.3417-10_3417delinsC | ||
| XM_006715412.2:c.3417-10_3417delinsC | ||
| XM_006715413.2:c.3417-10_3417delinsC | ||
| XM_006715415.2:c.3417-10_3417delinsC | ||
| XM_006715416.2:c.3417-10_3417delinsC | ||
| XM_006715417.2:c.3417-10_3417delinsC | ||
| XM_006715420.2:c.3417-10_3417delinsC | ||
| XM_006715421.2:c.3417-10_3417delinsC | ||
| XM_006715423.2:c.3417-10_3417delinsC | ||
| XM_006715424.2:c.3417-10_3417delinsC | ||
| XM_006715425.2:c.3417-10_3417delinsC | ||
| XM_011535641.2:c.3417-10_3417delinsC | ||
| XM_011535642.2:c.3417-10_3417delinsC | ||
| XM_011535645.2:c.1185-10_1185delinsC | ||
| XM_017010608.1:c.3417-10_3417delinsC | ||
| XM_017010609.1:c.3417-10_3417delinsC | ||
| XM_017010610.1:c.3396-10_3396delinsC | ||
| XM_017010611.2:c.3390-10_3390delinsC | ||
| XM_017010612.1:c.3339-10_3339delinsC | ||
| XM_017010613.1:c.3417-10_3417delinsC | ||
| XM_017010614.1:c.3417-10_3417delinsC | ||
| XM_017010615.1:c.3417-10_3417delinsC | ||
| XM_017010616.1:c.3417-10_3417delinsC | ||
| XM_017010617.1:c.3417-10_3417delinsC | ||
| XM_017010618.1:c.3417-10_3417delinsC | ||
| XM_017010619.1:c.1692-10_1692delinsC | ||
| XR_001743287.1:n.3900-10_3900delinsC | ||
| NM_182961.4:c.3396-10_3396delinsC | ||
| NM_033071.5:c.3417-10_3417delinsC |