Canonical Allele Identifier: CA1748622833

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142750542A= , CM000669.2:g.142750542A=	GRCh38
NC_000007.13:g.142458393A= , CM000669.1:g.142458393A=	GRCh37
NC_000007.12:g.142137967A=	NCBI36
NG_008307.3:g.6059A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000311737.12:c.41-13A= (PRSS1) MANE Select	ENSP00000308720.7:n.41-13A=
ENST00000311737.11:c.41-13A= (PRSS1)	ENSP00000308720.7:n.41-13A=
ENST00000485223.1:n.54-87A= (PRSS1)
ENST00000486171.5:c.41-13A= (PRSS1)	ENSP00000417854.1:n.41-13A=
ENST00000497041.1:n.45-13A= (PRSS1)
ENST00000610416.2:c.370+29356A= (TRBC1)	ENSP00000482915.1:n.370+29356A=
ENST00000612126.4:c.41-13A= (PRSS1)	ENSP00000479959.1:n.41-13A=
ENST00000619214.4:c.41-13A= (PRSS1)	ENSP00000481361.1:n.41-13A=
ENST00000633114.1:c.41-13A= (PRSS2)	ENSP00000487822.1:n.41-13A=
ENST00000634019.1:c.82+1751A= (PRSS2)	ENSP00000488594.1:n.82+1751A=
NM_002769.4:c.41-13A= (PRSS1)	NP_002760.1:n.41-13A=
XM_011516411.1:c.716-13A= (PRSS1)	XP_011514713.1:n.716-13A=
NM_002769.5:c.41-13A= (PRSS1) MANE Select	NP_002760.1:n.41-13A=
NR_172947.1:n.54-13A= (PRSS1)
NR_172948.1:n.54-13A= (PRSS1)
NR_172949.1:n.54-87A= (PRSS1)
NR_172950.1:n.53+1018A= (PRSS1)
NR_172951.1:n.54-87A= (PRSS1)