Canonical Allele Identifier: CA369608791

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• dbSNP Id: rs1798768921
• gnomAD v3: 7-142751891-T-G
• gnomAD v4: 7-142751891-T-G
• MyVariant Identifiers: chr7:g.142459742T>G (hg19) ; chr7:g.142751891T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751891T>G , CM000669.2:g.142751891T>G	GRCh38
NC_000007.13:g.142459742T>G , CM000669.1:g.142459742T>G	GRCh37
NC_000007.12:g.142139316T>G	NCBI36
NG_008307.3:g.7408T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.318T>G (PRSS1) MANE Select	ENSP00000308720.7:p.Asn106Lys
ENST00000311737.11:c.318T>G (PRSS1)	ENSP00000308720.7:p.Asn106Lys
ENST00000463701.1:n.782T>G (PRSS1)
ENST00000485223.1:n.1316T>G (PRSS1)
ENST00000486171.5:c.360T>G (PRSS1)	ENSP00000417854.1:p.Asn120Lys
ENST00000492062.1:c.168T>G (PRSS1)	ENSP00000419912.1:p.Asn56Lys
ENST00000610416.2:c.370+30705T>G (TRBC1)	ENSP00000482915.1:n.370+30705T>G
ENST00000612126.4:c.318T>G (PRSS1)	ENSP00000479959.1:p.Asn106Lys
ENST00000619214.4:c.288T>G (PRSS1)	ENSP00000481361.1:p.Asn96Lys
ENST00000633114.1:c.318T>G (PRSS2)	ENSP00000487822.1:p.Asn106Lys
ENST00000634019.1:c.82+3100T>G (PRSS2)	ENSP00000488594.1:n.82+3100T>G
NM_002769.4:c.318T>G (PRSS1)	NP_002760.1:p.Asn106Lys
XM_011516411.1:c.993T>G (PRSS1)	XP_011514713.1:p.Asn331Lys
NM_002769.5:c.318T>G (PRSS1) MANE Select	NP_002760.1:p.Asn106Lys
NR_172947.1:n.260T>G (PRSS1)
NR_172948.1:n.257T>G (PRSS1)
NR_172949.1:n.257T>G (PRSS1)
NR_172950.1:n.171T>G (PRSS1)
NR_172951.1:n.140-35T>G (PRSS1)