Canonical Allele Identifier: CA1748623719

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752016C= , CM000669.2:g.142752016C=	GRCh38
NC_000007.13:g.142459867C= , CM000669.1:g.142459867C=	GRCh37
NC_000007.12:g.142139441C=	NCBI36
NG_008307.3:g.7533C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.443C= (PRSS1) MANE Select	ENSP00000308720.7:p.Ala148=
ENST00000311737.11:c.443C= (PRSS1)	ENSP00000308720.7:p.Ala148=
ENST00000463701.1:n.907C= (PRSS1)
ENST00000486171.5:c.485C= (PRSS1)	ENSP00000417854.1:p.Ala162=
ENST00000492062.1:c.293C= (PRSS1)	ENSP00000419912.1:p.Ala98=
ENST00000610416.2:c.370+30830C= (TRBC1)	ENSP00000482915.1:n.370+30830C=
ENST00000612126.4:c.443C= (PRSS1)	ENSP00000479959.1:p.Ala148=
ENST00000619214.4:c.413C= (PRSS1)	ENSP00000481361.1:p.Ala138=
ENST00000633114.1:c.321+122C= (PRSS2)	ENSP00000487822.1:n.321+122C=
ENST00000634019.1:c.82+3225C= (PRSS2)	ENSP00000488594.1:n.82+3225C=
NM_002769.4:c.443C= (PRSS1)	NP_002760.1:p.Ala148=
XM_011516411.1:c.1118C= (PRSS1)	XP_011514713.1:p.Ala373=
NM_002769.5:c.443C= (PRSS1) MANE Select	NP_002760.1:p.Ala148=
NR_172947.1:n.385C= (PRSS1)
NR_172948.1:n.382C= (PRSS1)
NR_172949.1:n.382C= (PRSS1)
NR_172950.1:n.296C= (PRSS1)
NR_172951.1:n.230C= (PRSS1)