Canonical Allele Identifier: CA1748624387

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751911T= , CM000669.2:g.142751911T=	GRCh38
NC_000007.13:g.142459762T= , CM000669.1:g.142459762T=	GRCh37
NC_000007.12:g.142139336T=	NCBI36
NG_008307.3:g.7428T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.338T= (PRSS1) MANE Select	ENSP00000308720.7:p.Leu113=
ENST00000311737.11:c.338T= (PRSS1)	ENSP00000308720.7:p.Leu113=
ENST00000463701.1:n.802T= (PRSS1)
ENST00000485223.1:n.1336T= (PRSS1)
ENST00000486171.5:c.380T= (PRSS1)	ENSP00000417854.1:p.Leu127=
ENST00000492062.1:c.188T= (PRSS1)	ENSP00000419912.1:p.Leu63=
ENST00000610416.2:c.370+30725T= (TRBC1)	ENSP00000482915.1:n.370+30725T=
ENST00000612126.4:c.338T= (PRSS1)	ENSP00000479959.1:p.Leu113=
ENST00000619214.4:c.308T= (PRSS1)	ENSP00000481361.1:p.Leu103=
ENST00000633114.1:c.321+17T= (PRSS2)	ENSP00000487822.1:n.321+17T=
ENST00000634019.1:c.82+3120T= (PRSS2)	ENSP00000488594.1:n.82+3120T=
NM_002769.4:c.338T= (PRSS1)	NP_002760.1:p.Leu113=
XM_011516411.1:c.1013T= (PRSS1)	XP_011514713.1:p.Leu338=
NM_002769.5:c.338T= (PRSS1) MANE Select	NP_002760.1:p.Leu113=
NR_172947.1:n.280T= (PRSS1)
NR_172948.1:n.277T= (PRSS1)
NR_172949.1:n.277T= (PRSS1)
NR_172950.1:n.191T= (PRSS1)
NR_172951.1:n.140-15T= (PRSS1)