Canonical Allele Identifier: CA1748624366

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142751895A= , CM000669.2:g.142751895A= GRCh38
NC_000007.13:g.142459746A= , CM000669.1:g.142459746A= GRCh37
NC_000007.12:g.142139320A= NCBI36
NG_008307.3:g.7412A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311737.12:c.322A= (PRSS1) MANE Select ENSP00000308720.7:p.Ile108=
ENST00000311737.11:c.322A= (PRSS1) ENSP00000308720.7:p.Ile108=
ENST00000463701.1:n.786A= (PRSS1)
ENST00000485223.1:n.1320A= (PRSS1)
ENST00000486171.5:c.364A= (PRSS1) ENSP00000417854.1:p.Ile122=
ENST00000492062.1:c.172A= (PRSS1) ENSP00000419912.1:p.Ile58=
ENST00000610416.2:c.370+30709A= (TRBC1) ENSP00000482915.1:n.370+30709A=
ENST00000612126.4:c.322A= (PRSS1) ENSP00000479959.1:p.Ile108=
ENST00000619214.4:c.292A= (PRSS1) ENSP00000481361.1:p.Ile98=
ENST00000633114.1:c.321+1A= (PRSS2) ENSP00000487822.1:n.321+1A=
ENST00000634019.1:c.82+3104A= (PRSS2) ENSP00000488594.1:n.82+3104A=
NM_002769.4:c.322A= (PRSS1) NP_002760.1:p.Ile108=
XM_011516411.1:c.997A= (PRSS1) XP_011514713.1:p.Ile333=
NM_002769.5:c.322A= (PRSS1) MANE Select NP_002760.1:p.Ile108=
NR_172947.1:n.264A= (PRSS1)
NR_172948.1:n.261A= (PRSS1)
NR_172949.1:n.261A= (PRSS1)
NR_172950.1:n.175A= (PRSS1)
NR_172951.1:n.140-31A= (PRSS1)