Linked Data
dbSNP Id:
rs1415624897
gnomAD v2:
7-142459725-A-AGCC
MyVariant Identifiers:
chr7:g.142459725_142459726insGCC (hg19)
chr7:g.142751874_142751875insGCC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.142751875_142751876insCCG , CM000669.2:g.142751875_142751876insCCG | GRCh38 |
| NC_000007.13:g.142459726_142459727insCCG , CM000669.1:g.142459726_142459727insCCG | GRCh37 |
| NC_000007.12:g.142139300_142139301insCCG | NCBI36 |
| NG_008307.3:g.7392_7393insCCG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000311737.12:c.302_303insCCG (PRSS1) MANE Select | ENSP00000308720.7:p.Asp100_Arg101insSer | |
| ENST00000311737.11:c.302_303insCCG (PRSS1) | ENSP00000308720.7:p.Asp100_Arg101insSer | |
| ENST00000463701.1:n.766_767insCCG (PRSS1) | ||
| ENST00000485223.1:n.1300_1301insCCG (PRSS1) | ||
| ENST00000486171.5:c.344_345insCCG (PRSS1) | ENSP00000417854.1:p.Asp114_Arg115insSer | |
| ENST00000492062.1:c.152_153insCCG (PRSS1) | ENSP00000419912.1:p.Asp50_Arg51insSer | |
| ENST00000610416.2:c.370+30689_370+30690insCCG (TRBC1) | ENSP00000482915.1:n.370+30689_370+30690in... | |
| ENST00000612126.4:c.302_303insCCG (PRSS1) | ENSP00000479959.1:p.Asp100_Arg101insSer | |
| ENST00000619214.4:c.272_273insCCG (PRSS1) | ENSP00000481361.1:p.Asp90_Arg91insSer | |
| ENST00000633114.1:c.302_303insCCG (PRSS2) | ENSP00000487822.1:p.Asp100_Arg101insSer | |
| ENST00000634019.1:c.82+3084_82+3085insCCG (PRSS2) | ENSP00000488594.1:n.82+3084_82+3085insCCG... | |
| NM_002769.4:c.302_303insCCG (PRSS1) | NP_002760.1:p.Asp100_Arg101insSer | |
| XM_011516411.1:c.977_978insCCG (PRSS1) | XP_011514713.1:p.Asp325_Arg326insSer | |
| NM_002769.5:c.302_303insCCG (PRSS1) MANE Select | NP_002760.1:p.Asp100_Arg101insSer | |
| NR_172947.1:n.244_245insCCG (PRSS1) | ||
| NR_172948.1:n.241_242insCCG (PRSS1) | ||
| NR_172949.1:n.241_242insCCG (PRSS1) | ||
| NR_172950.1:n.155_156insCCG (PRSS1) | ||
| NR_172951.1:n.140-51_140-50insCCG (PRSS1) |