Linked Data
ClinVar Variation Id:
38363
dbSNP Id:
rs202003805
ExAC:
7:142458412 C / T
gnomAD v2:
7-142458412-C-T
gnomAD v3:
7-142750561-C-T
gnomAD v4:
7-142750561-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.142750561C>T , CM000669.2:g.142750561C>T | GRCh38 |
| NC_000007.13:g.142458412C>T , CM000669.1:g.142458412C>T | GRCh37 |
| NC_000007.12:g.142137986C>T | NCBI36 |
| NG_008307.3:g.6078C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000311737.12:c.47C>T (PRSS1) MANE Select | ENSP00000308720.7:p.Ala16Val | |
| ENST00000311737.11:c.47C>T (PRSS1) | ENSP00000308720.7:p.Ala16Val | |
| ENST00000485223.1:n.54-68C>T (PRSS1) | ||
| ENST00000486171.5:c.47C>T (PRSS1) | ENSP00000417854.1:p.Ala16Val | |
| ENST00000497041.1:n.51C>T (PRSS1) | ||
| ENST00000610416.2:c.370+29375C>T (TRBC1) | ENSP00000482915.1:n.370+29375C>T | |
| ENST00000612126.4:c.47C>T (PRSS1) | ENSP00000479959.1:p.Ala16Val | |
| ENST00000619214.4:c.47C>T (PRSS1) | ENSP00000481361.1:p.Ala16Val | |
| ENST00000633114.1:c.47C>T (PRSS2) | ENSP00000487822.1:p.Ala16Val | |
| ENST00000634019.1:c.82+1770C>T (PRSS2) | ENSP00000488594.1:n.82+1770C>T | |
| NM_002769.4:c.47C>T (PRSS1) | NP_002760.1:p.Ala16Val | |
| XM_011516411.1:c.722C>T (PRSS1) | XP_011514713.1:p.Ala241Val | |
| NM_002769.5:c.47C>T (PRSS1) MANE Select | NP_002760.1:p.Ala16Val | |
| NR_172947.1:n.60C>T (PRSS1) | ||
| NR_172948.1:n.60C>T (PRSS1) | ||
| NR_172949.1:n.54-68C>T (PRSS1) | ||
| NR_172950.1:n.53+1037C>T (PRSS1) | ||
| NR_172951.1:n.54-68C>T (PRSS1) |