Canonical Allele Identifier: CA1748624334

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751878A= , CM000669.2:g.142751878A=	GRCh38
NC_000007.13:g.142459729A= , CM000669.1:g.142459729A=	GRCh37
NC_000007.12:g.142139303A=	NCBI36
NG_008307.3:g.7395A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000311737.12:c.305A= (PRSS1) MANE Select	ENSP00000308720.7:p.Lys102=
ENST00000311737.11:c.305A= (PRSS1)	ENSP00000308720.7:p.Lys102=
ENST00000463701.1:n.769A= (PRSS1)
ENST00000485223.1:n.1303A= (PRSS1)
ENST00000486171.5:c.347A= (PRSS1)	ENSP00000417854.1:p.Lys116=
ENST00000492062.1:c.155A= (PRSS1)	ENSP00000419912.1:p.Lys52=
ENST00000610416.2:c.370+30692A= (TRBC1)	ENSP00000482915.1:n.370+30692A=
ENST00000612126.4:c.305A= (PRSS1)	ENSP00000479959.1:p.Lys102=
ENST00000619214.4:c.275A= (PRSS1)	ENSP00000481361.1:p.Lys92=
ENST00000633114.1:c.305A= (PRSS2)	ENSP00000487822.1:p.Lys102=
ENST00000634019.1:c.82+3087A= (PRSS2)	ENSP00000488594.1:n.82+3087A=
NM_002769.4:c.305A= (PRSS1)	NP_002760.1:p.Lys102=
XM_011516411.1:c.980A= (PRSS1)	XP_011514713.1:p.Lys327=
NM_002769.5:c.305A= (PRSS1) MANE Select	NP_002760.1:p.Lys102=
NR_172947.1:n.247A= (PRSS1)
NR_172948.1:n.244A= (PRSS1)
NR_172949.1:n.244A= (PRSS1)
NR_172950.1:n.158A= (PRSS1)
NR_172951.1:n.140-48A= (PRSS1)