Canonical Allele Identifier: CA1748622838

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142750549_142750550delinsCT , CM000669.2:g.142750549_142750550delinsCT	GRCh38
NC_000007.13:g.142458400_142458401delinsCT , CM000669.1:g.142458400_142458401delinsCT	GRCh37
NC_000007.12:g.142137974_142137975delinsCT	NCBI36
NG_008307.3:g.6066_6067delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000311737.12:c.41-6_41-5delinsCT (PRSS1) MANE Select	ENSP00000308720.7:n.41-6_41-5delinsCT
ENST00000311737.11:c.41-6_41-5delinsCT (PRSS1)	ENSP00000308720.7:n.41-6_41-5delinsCT
ENST00000485223.1:n.54-80_54-79delinsCT (PRSS1)
ENST00000486171.5:c.41-6_41-5delinsCT (PRSS1)	ENSP00000417854.1:n.41-6_41-5delinsCT
ENST00000497041.1:n.45-6_45-5delinsCT (PRSS1)
ENST00000610416.2:c.370+29363_370+29364delinsCT (TRBC1)	ENSP00000482915.1:n.370+29363_370+29364de...
ENST00000612126.4:c.41-6_41-5delinsCT (PRSS1)	ENSP00000479959.1:n.41-6_41-5delinsCT
ENST00000619214.4:c.41-6_41-5delinsCT (PRSS1)	ENSP00000481361.1:n.41-6_41-5delinsCT
ENST00000633114.1:c.41-6_41-5delinsCT (PRSS2)	ENSP00000487822.1:n.41-6_41-5delinsCT
ENST00000634019.1:c.82+1758_82+1759delinsCT (PRSS2)	ENSP00000488594.1:n.82+1758_82+1759delins...
NM_002769.4:c.41-6_41-5delinsCT (PRSS1)	NP_002760.1:n.41-6_41-5delinsCT
XM_011516411.1:c.716-6_716-5delinsCT (PRSS1)	XP_011514713.1:n.716-6_716-5delinsCT
NM_002769.5:c.41-6_41-5delinsCT (PRSS1) MANE Select	NP_002760.1:n.41-6_41-5delinsCT
NR_172947.1:n.54-6_54-5delinsCT (PRSS1)
NR_172948.1:n.54-6_54-5delinsCT (PRSS1)
NR_172949.1:n.54-80_54-79delinsCT (PRSS1)
NR_172950.1:n.53+1025_53+1026delinsCT (PRSS1)
NR_172951.1:n.54-80_54-79delinsCT (PRSS1)