Canonical Allele Identifier: CA4529931

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• ClinVar Variation Id: 1732350
• ClinVar RCV Id: RCV002459396
• dbSNP Id: rs766098231
• ExAC: 7:142459776 G / A
• gnomAD v2: 7-142459776-G-A
• MyVariant Identifiers: chr7:g.142459776G>A (hg19) ; chr7:g.142751925G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751925G>A , CM000669.2:g.142751925G>A	GRCh38
NC_000007.13:g.142459776G>A , CM000669.1:g.142459776G>A	GRCh37
NC_000007.12:g.142139350G>A	NCBI36
NG_008307.3:g.7442G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.352G>A (PRSS1) MANE Select	ENSP00000308720.7:p.Val118Ile
ENST00000311737.11:c.352G>A (PRSS1)	ENSP00000308720.7:p.Val118Ile
ENST00000463701.1:n.816G>A (PRSS1)
ENST00000485223.1:n.1350G>A (PRSS1)
ENST00000486171.5:c.394G>A (PRSS1)	ENSP00000417854.1:p.Val132Ile
ENST00000492062.1:c.202G>A (PRSS1)	ENSP00000419912.1:p.Val68Ile
ENST00000610416.2:c.370+30739G>A (TRBC1)	ENSP00000482915.1:n.370+30739G>A
ENST00000612126.4:c.352G>A (PRSS1)	ENSP00000479959.1:p.Val118Ile
ENST00000619214.4:c.322G>A (PRSS1)	ENSP00000481361.1:p.Val108Ile
ENST00000633114.1:c.321+31G>A (PRSS2)	ENSP00000487822.1:n.321+31G>A
ENST00000634019.1:c.82+3134G>A (PRSS2)	ENSP00000488594.1:n.82+3134G>A
NM_002769.4:c.352G>A (PRSS1)	NP_002760.1:p.Val118Ile
XM_011516411.1:c.1027G>A (PRSS1)	XP_011514713.1:p.Val343Ile
NM_002769.5:c.352G>A (PRSS1) MANE Select	NP_002760.1:p.Val118Ile
NR_172947.1:n.294G>A (PRSS1)
NR_172948.1:n.291G>A (PRSS1)
NR_172949.1:n.291G>A (PRSS1)
NR_172950.1:n.205G>A (PRSS1)
NR_172951.1:n.140-1G>A (PRSS1)