Linked Data
ClinVar Variation Id:
234529
dbSNP Id:
rs567739104
gnomAD v2:
10-89623280-C-T
gnomAD v3:
10-87863523-C-T
gnomAD v4:
10-87863523-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87863523C>T , CM000672.2:g.87863523C>T | GRCh38 |
| NC_000010.10:g.89623280C>T , CM000672.1:g.89623280C>T | GRCh37 |
| NC_000010.9:g.89613260C>T | NCBI36 |
| NG_007466.2:g.5086C>T , LRG_311:g.5086C>T | |
| NG_033079.1:g.4915G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706954.1:c.-17+881C>T (PTEN) | ENSP00000516674.1:n.-17+881C>T | |
| ENST00000688308.1:c.-17+410C>T (PTEN) | ENSP00000508752.1:n.-17+410C>T | |
| ENST00000693560.1:c.-427C>T (PTEN) | ENSP00000509861.1:n.-427C>T | |
| ENST00000445946.5:c.-1036G>A (KLLN) MANE Select | ENSP00000392204.2:n.-1036G>A | |
| ENST00000371953.7:c.-947C>T (PTEN) | ENSP00000361021.3:n.-947C>T | |
| ENST00000610634.1:c.-1049C>T (PTEN) | ENSP00000477517.1:n.-1049C>T | |
| NM_000314.5:c.-946C>T (PTEN) | NP_000305.3:n.-946C>T | |
| NM_000314.6:c.-946C>T (PTEN) | NP_000305.3:n.-946C>T | |
| NM_001304717.2:c.-427C>T (PTEN) | NP_001291646.2:n.-427C>T | |
| NM_001304718.1:c.-1651C>T (PTEN) | NP_001291647.1:n.-1651C>T | |
| NM_001126049.2:c.-1036G>A (KLLN) MANE Select | NP_001119521.1:n.-1036G>A |