Canonical Allele Identifier: CA1748624721

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753051A= , CM000669.2:g.142753051A= GRCh38
NC_000007.13:g.142460902A= , CM000669.1:g.142460902A= GRCh37
NC_000007.12:g.142140476A= NCBI36
NG_008307.3:g.8568A=

Transcript Alleles

HGVS Amino-acid change
ENST00000311737.12:c.*31A= (PRSS1) MANE Select ENSP00000308720.7:n.*31A=
ENST00000311737.11:c.*31A= (PRSS1) ENSP00000308720.7:n.*31A=
ENST00000463701.1:n.1239A= (PRSS1)
ENST00000492062.1:c.608A= (PRSS1) ENSP00000419912.1:n.608A=
ENST00000610416.2:c.370+31865A= (TRBC1) ENSP00000482915.1:n.370+31865A=
ENST00000612126.4:c.591+484A= (PRSS1) ENSP00000479959.1:n.591+484A=
ENST00000619214.4:c.*31A= (PRSS1) ENSP00000481361.1:n.*31A=
ENST00000633114.1:c.321+1157A= (PRSS2) ENSP00000487822.1:n.321+1157A=
ENST00000634019.1:c.82+4260A= (PRSS2) ENSP00000488594.1:n.82+4260A=
NM_002769.4:c.*31A= (PRSS1) NP_002760.1:n.*31A=
XM_011516411.1:c.*31A= (PRSS1) XP_011514713.1:n.*31A=
NM_002769.5:c.*31A= (PRSS1) MANE Select NP_002760.1:n.*31A=
NR_172947.1:n.717A= (PRSS1)
NR_172948.1:n.714A= (PRSS1)
NR_172949.1:n.714A= (PRSS1)
NR_172950.1:n.628A= (PRSS1)
NR_172951.1:n.562A= (PRSS1)