Canonical Allele Identifier: CA1108087457

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• gnomAD v3: 7-142749787-C-CT
• gnomAD v4: 7-142749787-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142749787_142749788insT , CM000669.2:g.142749787_142749788insT	GRCh38
NC_000007.13:g.142457638_142457639insT , CM000669.1:g.142457638_142457639insT	GRCh37
NC_000007.12:g.142137212_142137213insT	NCBI36
NG_008307.3:g.5304_5305insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.40+263_40+264insT (PRSS1) MANE Select	ENSP00000308720.7:n.40+263_40+264insT
ENST00000311737.11:c.40+263_40+264insT (PRSS1)	ENSP00000308720.7:n.40+263_40+264insT
ENST00000485223.1:n.53+263_53+264insT (PRSS1)
ENST00000486171.5:c.40+263_40+264insT (PRSS1)	ENSP00000417854.1:n.40+263_40+264insT
ENST00000497041.1:n.44+263_44+264insT (PRSS1)
ENST00000610416.2:c.370+28601_370+28602insT (TRBC1)	ENSP00000482915.1:n.370+28601_370+28602insT
ENST00000612126.4:c.40+263_40+264insT (PRSS1)	ENSP00000479959.1:n.40+263_40+264insT
ENST00000619214.4:c.40+263_40+264insT (PRSS1)	ENSP00000481361.1:n.40+263_40+264insT
ENST00000633114.1:c.40+263_40+264insT (PRSS2)	ENSP00000487822.1:n.40+263_40+264insT
ENST00000634019.1:c.82+996_82+997insT (PRSS2)	ENSP00000488594.1:n.82+996_82+997insT
NM_002769.4:c.40+263_40+264insT (PRSS1)	NP_002760.1:n.40+263_40+264insT
XM_011516411.1:c.715+263_715+264insT (PRSS1)	XP_011514713.1:n.715+263_715+264insT
NM_002769.5:c.40+263_40+264insT (PRSS1) MANE Select	NP_002760.1:n.40+263_40+264insT
NR_172947.1:n.53+263_53+264insT (PRSS1)
NR_172948.1:n.53+263_53+264insT (PRSS1)
NR_172949.1:n.53+263_53+264insT (PRSS1)
NR_172950.1:n.53+263_53+264insT (PRSS1)
NR_172951.1:n.53+263_53+264insT (PRSS1)