Canonical Allele Identifier: CA2715878488
Gene: PRSS1 HGNC NCBI
TRBC1 HGNC NCBI
PRSS2 HGNC NCBI

Linked Data

dbSNP Id: rs2116958024
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142750449_142750450del , CM000669.2:g.142750449_142750450del GRCh38
NC_000007.13:g.142458300_142458301del , CM000669.1:g.142458300_142458301del GRCh37
NC_000007.12:g.142137874_142137875del NCBI36
NG_008307.3:g.5966_5967del

Transcript Alleles

HGVS Amino-acid change
ENST00000311737.12:c.41-106_41-105del (PRSS1) MANE Select ENSP00000308720.7:n.41-106_41-105del
ENST00000311737.11:c.41-106_41-105del (PRSS1) ENSP00000308720.7:n.41-106_41-105del
ENST00000485223.1:n.54-180_54-179del (PRSS1)
ENST00000486171.5:c.41-106_41-105del (PRSS1) ENSP00000417854.1:n.41-106_41-105del
ENST00000497041.1:n.45-106_45-105del (PRSS1)
ENST00000610416.2:c.370+29263_370+29264del (TRBC1) ENSP00000482915.1:n.370+29263_370+29264del
ENST00000612126.4:c.41-106_41-105del (PRSS1) ENSP00000479959.1:n.41-106_41-105del
ENST00000619214.4:c.41-106_41-105del (PRSS1) ENSP00000481361.1:n.41-106_41-105del
ENST00000633114.1:c.41-106_41-105del (PRSS2) ENSP00000487822.1:n.41-106_41-105del
ENST00000634019.1:c.82+1658_82+1659del (PRSS2) ENSP00000488594.1:n.82+1658_82+1659del
NM_002769.4:c.41-106_41-105del (PRSS1) NP_002760.1:n.41-106_41-105del
XM_011516411.1:c.716-106_716-105del (PRSS1) XP_011514713.1:n.716-106_716-105del
NM_002769.5:c.41-106_41-105del (PRSS1) MANE Select NP_002760.1:n.41-106_41-105del
NR_172947.1:n.54-106_54-105del (PRSS1)
NR_172948.1:n.54-106_54-105del (PRSS1)
NR_172949.1:n.54-180_54-179del (PRSS1)
NR_172950.1:n.53+925_53+926del (PRSS1)
NR_172951.1:n.54-180_54-179del (PRSS1)
Search 100 bp 5'
Search 100 bp 3'