Canonical Allele Identifier: CA1748622736

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142750412_142750413delinsAC , CM000669.2:g.142750412_142750413delinsAC GRCh38
NC_000007.13:g.142458263_142458264delinsAC , CM000669.1:g.142458263_142458264delinsAC GRCh37
NC_000007.12:g.142137837_142137838delinsAC NCBI36
NG_008307.3:g.5929_5930delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000311737.12:c.41-143_41-142delinsAC (PRSS1) MANE Select ENSP00000308720.7:n.41-143_41-142delinsAC
ENST00000311737.11:c.41-143_41-142delinsAC (PRSS1) ENSP00000308720.7:n.41-143_41-142delinsAC
ENST00000485223.1:n.54-217_54-216delinsAC (PRSS1)
ENST00000486171.5:c.41-143_41-142delinsAC (PRSS1) ENSP00000417854.1:n.41-143_41-142delinsAC
ENST00000497041.1:n.45-143_45-142delinsAC (PRSS1)
ENST00000610416.2:c.370+29226_370+29227delinsAC (TRBC1) ENSP00000482915.1:n.370+29226_370+29227delinsAC
ENST00000612126.4:c.41-143_41-142delinsAC (PRSS1) ENSP00000479959.1:n.41-143_41-142delinsAC
ENST00000619214.4:c.41-143_41-142delinsAC (PRSS1) ENSP00000481361.1:n.41-143_41-142delinsAC
ENST00000633114.1:c.41-143_41-142delinsAC (PRSS2) ENSP00000487822.1:n.41-143_41-142delinsAC
ENST00000634019.1:c.82+1621_82+1622delinsAC (PRSS2) ENSP00000488594.1:n.82+1621_82+1622delinsAC
NM_002769.4:c.41-143_41-142delinsAC (PRSS1) NP_002760.1:n.41-143_41-142delinsAC
XM_011516411.1:c.716-143_716-142delinsAC (PRSS1) XP_011514713.1:n.716-143_716-142delinsAC
NM_002769.5:c.41-143_41-142delinsAC (PRSS1) MANE Select NP_002760.1:n.41-143_41-142delinsAC
NR_172947.1:n.54-143_54-142delinsAC (PRSS1)
NR_172948.1:n.54-143_54-142delinsAC (PRSS1)
NR_172949.1:n.54-217_54-216delinsAC (PRSS1)
NR_172950.1:n.53+888_53+889delinsAC (PRSS1)
NR_172951.1:n.54-217_54-216delinsAC (PRSS1)