Linked Data
ClinVar Variation Id:
141628
dbSNP Id:
rs564216039
gnomAD v3:
10-87863399-C-G
gnomAD v4:
10-87863399-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87863399C>G , CM000672.2:g.87863399C>G | GRCh38 |
| NC_000010.10:g.89623156C>G , CM000672.1:g.89623156C>G | GRCh37 |
| NC_000010.9:g.89613136C>G | NCBI36 |
| NG_007466.2:g.4962C>G , LRG_311:g.4962C>G | |
| NG_033079.1:g.5039G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706954.1:c.-17+757C>G (PTEN) | ENSP00000516674.1:n.-17+757C>G | |
| ENST00000688308.1:c.-17+286C>G (PTEN) | ENSP00000508752.1:n.-17+286C>G | |
| ENST00000445946.5:c.-912G>C (KLLN) MANE Select | ENSP00000392204.2:n.-912G>C | |
| ENST00000371953.7:c.-1071C>G (PTEN) | ENSP00000361021.3:n.-1071C>G | |
| ENST00000445946.3:c.-912G>C (KLLN) | ENSP00000392204.2:n.-912G>C | |
| NM_001126049.1:c.-912G>C (KLLN) | NP_001119521.1:n.-912G>C | |
| NM_001126049.2:c.-912G>C (KLLN) MANE Select | NP_001119521.1:n.-912G>C |