Linked Data
ClinVar Variation Id:
824993
ClinVar RCV Id:
RCV001862226
dbSNP Id:
rs766731858
ExAC:
7:142459878 G / A
gnomAD v2:
7-142459878-G-A
gnomAD v3:
7-142752027-G-A
gnomAD v4:
7-142752027-G-A
COSMIC:
COSM1086581
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.142752027G>A , CM000669.2:g.142752027G>A | GRCh38 |
| NC_000007.13:g.142459878G>A , CM000669.1:g.142459878G>A | GRCh37 |
| NC_000007.12:g.142139452G>A | NCBI36 |
| NG_008307.3:g.7544G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311737.12:c.454G>A (PRSS1) MANE Select | ENSP00000308720.7:p.Ala152Thr | |
| ENST00000311737.11:c.454G>A (PRSS1) | ENSP00000308720.7:p.Ala152Thr | |
| ENST00000463701.1:n.918G>A (PRSS1) | ||
| ENST00000486171.5:c.496G>A (PRSS1) | ENSP00000417854.1:p.Ala166Thr | |
| ENST00000492062.1:c.304G>A (PRSS1) | ENSP00000419912.1:p.Ala102Thr | |
| ENST00000610416.2:c.370+30841G>A (TRBC1) | ENSP00000482915.1:n.370+30841G>A | |
| ENST00000612126.4:c.454G>A (PRSS1) | ENSP00000479959.1:p.Ala152Thr | |
| ENST00000619214.4:c.424G>A (PRSS1) | ENSP00000481361.1:p.Ala142Thr | |
| ENST00000633114.1:c.321+133G>A (PRSS2) | ENSP00000487822.1:n.321+133G>A | |
| ENST00000634019.1:c.82+3236G>A (PRSS2) | ENSP00000488594.1:n.82+3236G>A | |
| NM_002769.4:c.454G>A (PRSS1) | NP_002760.1:p.Ala152Thr | |
| XM_011516411.1:c.1129G>A (PRSS1) | XP_011514713.1:p.Ala377Thr | |
| NM_002769.5:c.454G>A (PRSS1) MANE Select | NP_002760.1:p.Ala152Thr | |
| NR_172947.1:n.396G>A (PRSS1) | ||
| NR_172948.1:n.393G>A (PRSS1) | ||
| NR_172949.1:n.393G>A (PRSS1) | ||
| NR_172950.1:n.307G>A (PRSS1) | ||
| NR_172951.1:n.241G>A (PRSS1) |