Canonical Allele Identifier: CA1748624421

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751922G= , CM000669.2:g.142751922G=	GRCh38
NC_000007.13:g.142459773G= , CM000669.1:g.142459773G=	GRCh37
NC_000007.12:g.142139347G=	NCBI36
NG_008307.3:g.7439G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.349G= (PRSS1) MANE Select	ENSP00000308720.7:p.Ala117=
ENST00000311737.11:c.349G= (PRSS1)	ENSP00000308720.7:p.Ala117=
ENST00000463701.1:n.813G= (PRSS1)
ENST00000485223.1:n.1347G= (PRSS1)
ENST00000486171.5:c.391G= (PRSS1)	ENSP00000417854.1:p.Ala131=
ENST00000492062.1:c.199G= (PRSS1)	ENSP00000419912.1:p.Ala67=
ENST00000610416.2:c.370+30736G= (TRBC1)	ENSP00000482915.1:n.370+30736G=
ENST00000612126.4:c.349G= (PRSS1)	ENSP00000479959.1:p.Ala117=
ENST00000619214.4:c.319G= (PRSS1)	ENSP00000481361.1:p.Ala107=
ENST00000633114.1:c.321+28G= (PRSS2)	ENSP00000487822.1:n.321+28G=
ENST00000634019.1:c.82+3131G= (PRSS2)	ENSP00000488594.1:n.82+3131G=
NM_002769.4:c.349G= (PRSS1)	NP_002760.1:p.Ala117=
XM_011516411.1:c.1024G= (PRSS1)	XP_011514713.1:p.Ala342=
NM_002769.5:c.349G= (PRSS1) MANE Select	NP_002760.1:p.Ala117=
NR_172947.1:n.291G= (PRSS1)
NR_172948.1:n.288G= (PRSS1)
NR_172949.1:n.288G= (PRSS1)
NR_172950.1:n.202G= (PRSS1)
NR_172951.1:n.140-4G= (PRSS1)