Canonical Allele Identifier: CA1748624468

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751937C= , CM000669.2:g.142751937C=	GRCh38
NC_000007.13:g.142459788C= , CM000669.1:g.142459788C=	GRCh37
NC_000007.12:g.142139362C=	NCBI36
NG_008307.3:g.7454C=

Transcript Alleles

HGVS	Amino-acid Change
NM_002769.5:c.364C= (PRSS1) MANE Select	NP_002760.1:p.Arg122=
ENST00000311737.12:c.364C= (PRSS1) MANE Select	ENSP00000308720.7:p.Arg122=
NM_002769.4:c.364C= (PRSS1)	NP_002760.1:p.Arg122=
NR_172947.1:n.306C= (PRSS1)
NR_172948.1:n.303C= (PRSS1)
NR_172949.1:n.303C= (PRSS1)
NR_172950.1:n.217C= (PRSS1)
NR_172951.1:n.151C= (PRSS1)
ENST00000311737.11:c.364C= (PRSS1)	ENSP00000308720.7:p.Arg122=
ENST00000463701.1:n.828C= (PRSS1)
ENST00000485223.1:n.1362C= (PRSS1)
ENST00000486171.5:c.406C= (PRSS1)	ENSP00000417854.1:p.Arg136=
ENST00000492062.1:c.214C= (PRSS1)	ENSP00000419912.1:p.Arg72=
ENST00000610416.2:c.370+30751C= (TRBC1)	ENSP00000482915.1:n.370+30751C=
ENST00000612126.4:c.364C= (PRSS1)	ENSP00000479959.1:p.Arg122=
ENST00000619214.4:c.334C= (PRSS1)	ENSP00000481361.1:p.Arg112=
ENST00000633114.1:c.321+43C= (PRSS2)	ENSP00000487822.1:n.321+43C=
ENST00000634019.1:c.82+3146C= (PRSS2)	ENSP00000488594.1:n.82+3146C=
XM_011516411.1:c.1039C= (PRSS1)	XP_011514713.1:p.Arg347=