Canonical Allele Identifier: CA1748623633

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142751979G= , CM000669.2:g.142751979G= GRCh38
NC_000007.13:g.142459830G= , CM000669.1:g.142459830G= GRCh37
NC_000007.12:g.142139404G= NCBI36
NG_008307.3:g.7496G=

Transcript Alleles

HGVS Amino-acid change
ENST00000311737.12:c.406G= (PRSS1) MANE Select ENSP00000308720.7:p.Gly136=
ENST00000311737.11:c.406G= (PRSS1) ENSP00000308720.7:p.Gly136=
ENST00000463701.1:n.870G= (PRSS1)
ENST00000485223.1:n.1404G= (PRSS1)
ENST00000486171.5:c.448G= (PRSS1) ENSP00000417854.1:p.Gly150=
ENST00000492062.1:c.256G= (PRSS1) ENSP00000419912.1:p.Gly86=
ENST00000610416.2:c.370+30793G= (TRBC1) ENSP00000482915.1:n.370+30793G=
ENST00000612126.4:c.406G= (PRSS1) ENSP00000479959.1:p.Gly136=
ENST00000619214.4:c.376G= (PRSS1) ENSP00000481361.1:p.Gly126=
ENST00000633114.1:c.321+85G= (PRSS2) ENSP00000487822.1:n.321+85G=
ENST00000634019.1:c.82+3188G= (PRSS2) ENSP00000488594.1:n.82+3188G=
NM_002769.4:c.406G= (PRSS1) NP_002760.1:p.Gly136=
XM_011516411.1:c.1081G= (PRSS1) XP_011514713.1:p.Gly361=
NM_002769.5:c.406G= (PRSS1) MANE Select NP_002760.1:p.Gly136=
NR_172947.1:n.348G= (PRSS1)
NR_172948.1:n.345G= (PRSS1)
NR_172949.1:n.345G= (PRSS1)
NR_172950.1:n.259G= (PRSS1)
NR_172951.1:n.193G= (PRSS1)