Canonical Allele Identifier: CA1108079783

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• dbSNP Id: rs1798806196
• gnomAD v3: 7-142752240-G-GCT
• gnomAD v4: 7-142752240-G-GCT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752240_142752241insCT , CM000669.2:g.142752240_142752241insCT	GRCh38
NC_000007.13:g.142460091_142460092insCT , CM000669.1:g.142460091_142460092insCT	GRCh37
NC_000007.12:g.142139665_142139666insCT	NCBI36
NG_008307.3:g.7757_7758insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.455-191_455-190insCT (PRSS1) MANE Select	ENSP00000308720.7:n.455-191_455-190insCT
ENST00000311737.11:c.455-191_455-190insCT (PRSS1)	ENSP00000308720.7:n.455-191_455-190insCT
ENST00000463701.1:n.919-191_919-190insCT (PRSS1)
ENST00000486171.5:c.497-191_497-190insCT (PRSS1)	ENSP00000417854.1:n.497-191_497-190insCT
ENST00000492062.1:c.305-191_305-190insCT (PRSS1)	ENSP00000419912.1:n.305-191_305-190insCT
ENST00000610416.2:c.370+31054_370+31055insCT (TRBC1)	ENSP00000482915.1:n.370+31054_370+31055insCT
ENST00000612126.4:c.455-191_455-190insCT (PRSS1)	ENSP00000479959.1:n.455-191_455-190insCT
ENST00000619214.4:c.425-191_425-190insCT (PRSS1)	ENSP00000481361.1:n.425-191_425-190insCT
ENST00000633114.1:c.321+346_321+347insCT (PRSS2)	ENSP00000487822.1:n.321+346_321+347insCT
ENST00000634019.1:c.82+3449_82+3450insCT (PRSS2)	ENSP00000488594.1:n.82+3449_82+3450insCT
NM_002769.4:c.455-191_455-190insCT (PRSS1)	NP_002760.1:n.455-191_455-190insCT
XM_011516411.1:c.1130-191_1130-190insCT (PRSS1)	XP_011514713.1:n.1130-191_1130-190insCT
NM_002769.5:c.455-191_455-190insCT (PRSS1) MANE Select	NP_002760.1:n.455-191_455-190insCT
NR_172947.1:n.397-191_397-190insCT (PRSS1)
NR_172948.1:n.394-191_394-190insCT (PRSS1)
NR_172949.1:n.394-191_394-190insCT (PRSS1)
NR_172950.1:n.308-191_308-190insCT (PRSS1)
NR_172951.1:n.242-191_242-190insCT (PRSS1)