Canonical Allele Identifier: CA1748623988

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• dbSNP Id: rs1798801837

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752212_142752219dup , CM000669.2:g.142752212_142752219dup	GRCh38
NC_000007.13:g.142460063_142460070dup , CM000669.1:g.142460063_142460070dup	GRCh37
NC_000007.12:g.142139637_142139644dup	NCBI36
NG_008307.3:g.7729_7736dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.454+185_454+192dup (PRSS1) MANE Select	ENSP00000308720.7:n.454+185_454+192dup
ENST00000311737.11:c.454+185_454+192dup (PRSS1)	ENSP00000308720.7:n.454+185_454+192dup
ENST00000463701.1:n.918+185_918+192dup (PRSS1)
ENST00000486171.5:c.496+185_496+192dup (PRSS1)	ENSP00000417854.1:n.496+185_496+192dup
ENST00000492062.1:c.304+185_304+192dup (PRSS1)	ENSP00000419912.1:n.304+185_304+192dup
ENST00000610416.2:c.370+31026_370+31033dup (TRBC1)	ENSP00000482915.1:n.370+31026_370+31033dup
ENST00000612126.4:c.454+185_454+192dup (PRSS1)	ENSP00000479959.1:n.454+185_454+192dup
ENST00000619214.4:c.424+185_424+192dup (PRSS1)	ENSP00000481361.1:n.424+185_424+192dup
ENST00000633114.1:c.321+318_321+325dup (PRSS2)	ENSP00000487822.1:n.321+318_321+325dup
ENST00000634019.1:c.82+3421_82+3428dup (PRSS2)	ENSP00000488594.1:n.82+3421_82+3428dup
NM_002769.4:c.454+185_454+192dup (PRSS1)	NP_002760.1:n.454+185_454+192dup
XM_011516411.1:c.1129+185_1129+192dup (PRSS1)	XP_011514713.1:n.1129+185_1129+192dup
NM_002769.5:c.454+185_454+192dup (PRSS1) MANE Select	NP_002760.1:n.454+185_454+192dup
NR_172947.1:n.396+185_396+192dup (PRSS1)
NR_172948.1:n.393+185_393+192dup (PRSS1)
NR_172949.1:n.393+185_393+192dup (PRSS1)
NR_172950.1:n.307+185_307+192dup (PRSS1)
NR_172951.1:n.241+185_241+192dup (PRSS1)