Canonical Allele Identifier: CA2778215808

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142750560_142750563del , CM000669.2:g.142750560_142750563del GRCh38
NC_000007.13:g.142458411_142458414del , CM000669.1:g.142458411_142458414del GRCh37
NC_000007.12:g.142137985_142137988del NCBI36
NG_008307.3:g.6077_6080del

Transcript Alleles

HGVS Amino-acid Change
ENST00000311737.12:c.46_49del (PRSS1) MANE Select ENSP00000308720.7:p.Ala16ProfsTer25
ENST00000311737.11:c.46_49del (PRSS1) ENSP00000308720.7:p.Ala16ProfsTer25
ENST00000485223.1:n.54-69_54-66del (PRSS1)
ENST00000486171.5:c.46_49del (PRSS1) ENSP00000417854.1:p.Ala16ProfsTer25
ENST00000497041.1:n.50_53del (PRSS1)
ENST00000610416.2:c.370+29374_370+29377del (TRBC1) ENSP00000482915.1:n.370+29374_370+29377del
ENST00000612126.4:c.46_49del (PRSS1) ENSP00000479959.1:p.Ala16ProfsTer25
ENST00000619214.4:c.46_49del (PRSS1) ENSP00000481361.1:p.Ala16ProfsTer25
ENST00000633114.1:c.46_49del (PRSS2) ENSP00000487822.1:p.Ala16ProfsTer25
ENST00000634019.1:c.82+1769_82+1772del (PRSS2) ENSP00000488594.1:n.82+1769_82+1772del
NM_002769.4:c.46_49del (PRSS1) NP_002760.1:p.Ala16ProfsTer25
XM_011516411.1:c.721_724del (PRSS1) XP_011514713.1:p.Ala241ProfsTer25
NM_002769.5:c.46_49del (PRSS1) MANE Select NP_002760.1:p.Ala16ProfsTer25
NR_172947.1:n.59_62del (PRSS1)
NR_172948.1:n.59_62del (PRSS1)
NR_172949.1:n.54-69_54-66del (PRSS1)
NR_172950.1:n.53+1036_53+1039del (PRSS1)
NR_172951.1:n.54-69_54-66del (PRSS1)