Canonical Allele Identifier: CA1748623760

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752030G= , CM000669.2:g.142752030G=	GRCh38
NC_000007.13:g.142459881G= , CM000669.1:g.142459881G=	GRCh37
NC_000007.12:g.142139455G=	NCBI36
NG_008307.3:g.7547G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.454+3G= (PRSS1) MANE Select	ENSP00000308720.7:n.454+3G=
ENST00000311737.11:c.454+3G= (PRSS1)	ENSP00000308720.7:n.454+3G=
ENST00000463701.1:n.918+3G= (PRSS1)
ENST00000486171.5:c.496+3G= (PRSS1)	ENSP00000417854.1:n.496+3G=
ENST00000492062.1:c.304+3G= (PRSS1)	ENSP00000419912.1:n.304+3G=
ENST00000610416.2:c.370+30844G= (TRBC1)	ENSP00000482915.1:n.370+30844G=
ENST00000612126.4:c.454+3G= (PRSS1)	ENSP00000479959.1:n.454+3G=
ENST00000619214.4:c.424+3G= (PRSS1)	ENSP00000481361.1:n.424+3G=
ENST00000633114.1:c.321+136G= (PRSS2)	ENSP00000487822.1:n.321+136G=
ENST00000634019.1:c.82+3239G= (PRSS2)	ENSP00000488594.1:n.82+3239G=
NM_002769.4:c.454+3G= (PRSS1)	NP_002760.1:n.454+3G=
XM_011516411.1:c.1129+3G= (PRSS1)	XP_011514713.1:n.1129+3G=
NM_002769.5:c.454+3G= (PRSS1) MANE Select	NP_002760.1:n.454+3G=
NR_172947.1:n.396+3G= (PRSS1)
NR_172948.1:n.393+3G= (PRSS1)
NR_172949.1:n.393+3G= (PRSS1)
NR_172950.1:n.307+3G= (PRSS1)
NR_172951.1:n.241+3G= (PRSS1)