Canonical Allele Identifier: CA1748622391

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142749938G= , CM000669.2:g.142749938G=	GRCh38
NC_000007.13:g.142457789G= , CM000669.1:g.142457789G=	GRCh37
NC_000007.12:g.142137363G=	NCBI36
NG_008307.3:g.5455G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.40+414G= (PRSS1) MANE Select	ENSP00000308720.7:n.40+414G=
ENST00000311737.11:c.40+414G= (PRSS1)	ENSP00000308720.7:n.40+414G=
ENST00000485223.1:n.53+414G= (PRSS1)
ENST00000486171.5:c.40+414G= (PRSS1)	ENSP00000417854.1:n.40+414G=
ENST00000497041.1:n.44+414G= (PRSS1)
ENST00000610416.2:c.370+28752G= (TRBC1)	ENSP00000482915.1:n.370+28752G=
ENST00000612126.4:c.40+414G= (PRSS1)	ENSP00000479959.1:n.40+414G=
ENST00000619214.4:c.40+414G= (PRSS1)	ENSP00000481361.1:n.40+414G=
ENST00000633114.1:c.40+414G= (PRSS2)	ENSP00000487822.1:n.40+414G=
ENST00000634019.1:c.82+1147G= (PRSS2)	ENSP00000488594.1:n.82+1147G=
NM_002769.4:c.40+414G= (PRSS1)	NP_002760.1:n.40+414G=
XM_011516411.1:c.715+414G= (PRSS1)	XP_011514713.1:n.715+414G=
NM_002769.5:c.40+414G= (PRSS1) MANE Select	NP_002760.1:n.40+414G=
NR_172947.1:n.53+414G= (PRSS1)
NR_172948.1:n.53+414G= (PRSS1)
NR_172949.1:n.53+414G= (PRSS1)
NR_172950.1:n.53+414G= (PRSS1)
NR_172951.1:n.53+414G= (PRSS1)