Canonical Allele Identifier: CA4529876
Community Standard Title: NM_002769.5(PRSS1):c.202C>T (p.Arg68Cys)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142751775C>T , CM000669.2:g.142751775C>T GRCh38
NC_000007.13:g.142459626C>T , CM000669.1:g.142459626C>T GRCh37
NC_000007.12:g.142139200C>T NCBI36
NG_008307.3:g.7292C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002769.5:c.202C>T (PRSS1) MANE Select NP_002760.1:p.Arg68Cys
ENST00000311737.12:c.202C>T (PRSS1) MANE Select ENSP00000308720.7:p.Arg68Cys
NM_002769.4:c.202C>T (PRSS1) NP_002760.1:p.Arg68Cys
NR_172947.1:n.198-54C>T (PRSS1)
NR_172948.1:n.198-57C>T (PRSS1)
NR_172949.1:n.141C>T (PRSS1)
NR_172950.1:n.55C>T (PRSS1)
NR_172951.1:n.140-151C>T (PRSS1)
ENST00000311737.11:c.202C>T (PRSS1) ENSP00000308720.7:p.Arg68Cys
ENST00000463701.1:n.666C>T (PRSS1)
ENST00000485223.1:n.1200C>T (PRSS1)
ENST00000486171.5:c.244C>T (PRSS1) ENSP00000417854.1:p.Arg82Cys
ENST00000492062.1:c.52C>T (PRSS1) ENSP00000419912.1:p.Arg18Cys
ENST00000610416.2:c.370+30589C>T (TRBC1) ENSP00000482915.1:n.370+30589C>T
ENST00000612126.4:c.202C>T (PRSS1) ENSP00000479959.1:p.Arg68Cys
ENST00000619214.4:c.202C>T (PRSS1) ENSP00000481361.1:p.Arg68Cys
ENST00000633114.1:c.202C>T (PRSS2) ENSP00000487822.1:p.Arg68Cys
ENST00000634019.1:c.82+2984C>T (PRSS2) ENSP00000488594.1:n.82+2984C>T
XM_011516411.1:c.877C>T (PRSS1) XP_011514713.1:p.Arg293Cys