Canonical Allele Identifier: CA1748623613

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751971C= , CM000669.2:g.142751971C=	GRCh38
NC_000007.13:g.142459822C= , CM000669.1:g.142459822C=	GRCh37
NC_000007.12:g.142139396C=	NCBI36
NG_008307.3:g.7488C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.398C= (PRSS1) MANE Select	ENSP00000308720.7:p.Pro133=
ENST00000311737.11:c.398C= (PRSS1)	ENSP00000308720.7:p.Pro133=
ENST00000463701.1:n.862C= (PRSS1)
ENST00000485223.1:n.1396C= (PRSS1)
ENST00000486171.5:c.440C= (PRSS1)	ENSP00000417854.1:p.Pro147=
ENST00000492062.1:c.248C= (PRSS1)	ENSP00000419912.1:p.Pro83=
ENST00000610416.2:c.370+30785C= (TRBC1)	ENSP00000482915.1:n.370+30785C=
ENST00000612126.4:c.398C= (PRSS1)	ENSP00000479959.1:p.Pro133=
ENST00000619214.4:c.368C= (PRSS1)	ENSP00000481361.1:p.Pro123=
ENST00000633114.1:c.321+77C= (PRSS2)	ENSP00000487822.1:n.321+77C=
ENST00000634019.1:c.82+3180C= (PRSS2)	ENSP00000488594.1:n.82+3180C=
NM_002769.4:c.398C= (PRSS1)	NP_002760.1:p.Pro133=
XM_011516411.1:c.1073C= (PRSS1)	XP_011514713.1:p.Pro358=
NM_002769.5:c.398C= (PRSS1) MANE Select	NP_002760.1:p.Pro133=
NR_172947.1:n.340C= (PRSS1)
NR_172948.1:n.337C= (PRSS1)
NR_172949.1:n.337C= (PRSS1)
NR_172950.1:n.251C= (PRSS1)
NR_172951.1:n.185C= (PRSS1)