Canonical Allele Identifier: CA1748624142

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751779T= , CM000669.2:g.142751779T=	GRCh38
NC_000007.13:g.142459630T= , CM000669.1:g.142459630T=	GRCh37
NC_000007.12:g.142139204T=	NCBI36
NG_008307.3:g.7296T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.206T= (PRSS1) MANE Select	ENSP00000308720.7:p.Ile69=
ENST00000311737.11:c.206T= (PRSS1)	ENSP00000308720.7:p.Ile69=
ENST00000463701.1:n.670T= (PRSS1)
ENST00000485223.1:n.1204T= (PRSS1)
ENST00000486171.5:c.248T= (PRSS1)	ENSP00000417854.1:p.Ile83=
ENST00000492062.1:c.56T= (PRSS1)	ENSP00000419912.1:p.Ile19=
ENST00000610416.2:c.370+30593T= (TRBC1)	ENSP00000482915.1:n.370+30593T=
ENST00000612126.4:c.206T= (PRSS1)	ENSP00000479959.1:p.Ile69=
ENST00000619214.4:c.206T= (PRSS1)	ENSP00000481361.1:p.Ile69=
ENST00000633114.1:c.206T= (PRSS2)	ENSP00000487822.1:p.Ile69=
ENST00000634019.1:c.82+2988T= (PRSS2)	ENSP00000488594.1:n.82+2988T=
NM_002769.4:c.206T= (PRSS1)	NP_002760.1:p.Ile69=
XM_011516411.1:c.881T= (PRSS1)	XP_011514713.1:p.Ile294=
NM_002769.5:c.206T= (PRSS1) MANE Select	NP_002760.1:p.Ile69=
NR_172947.1:n.198-50T= (PRSS1)
NR_172948.1:n.198-53T= (PRSS1)
NR_172949.1:n.145T= (PRSS1)
NR_172950.1:n.59T= (PRSS1)
NR_172951.1:n.140-147T= (PRSS1)