Canonical Allele Identifier: CA1748624448

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751933C= , CM000669.2:g.142751933C=	GRCh38
NC_000007.13:g.142459784C= , CM000669.1:g.142459784C=	GRCh37
NC_000007.12:g.142139358C=	NCBI36
NG_008307.3:g.7450C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.360C= (PRSS1) MANE Select	ENSP00000308720.7:p.Asn120=
ENST00000311737.11:c.360C= (PRSS1)	ENSP00000308720.7:p.Asn120=
ENST00000463701.1:n.824C= (PRSS1)
ENST00000485223.1:n.1358C= (PRSS1)
ENST00000486171.5:c.402C= (PRSS1)	ENSP00000417854.1:p.Asn134=
ENST00000492062.1:c.210C= (PRSS1)	ENSP00000419912.1:p.Asn70=
ENST00000610416.2:c.370+30747C= (TRBC1)	ENSP00000482915.1:n.370+30747C=
ENST00000612126.4:c.360C= (PRSS1)	ENSP00000479959.1:p.Asn120=
ENST00000619214.4:c.330C= (PRSS1)	ENSP00000481361.1:p.Asn110=
ENST00000633114.1:c.321+39C= (PRSS2)	ENSP00000487822.1:n.321+39C=
ENST00000634019.1:c.82+3142C= (PRSS2)	ENSP00000488594.1:n.82+3142C=
NM_002769.4:c.360C= (PRSS1)	NP_002760.1:p.Asn120=
XM_011516411.1:c.1035C= (PRSS1)	XP_011514713.1:p.Asn345=
NM_002769.5:c.360C= (PRSS1) MANE Select	NP_002760.1:p.Asn120=
NR_172947.1:n.302C= (PRSS1)
NR_172948.1:n.299C= (PRSS1)
NR_172949.1:n.299C= (PRSS1)
NR_172950.1:n.213C= (PRSS1)
NR_172951.1:n.147C= (PRSS1)