Canonical Allele Identifier: CA2685348601

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• gnomAD v4: 7-142751952-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751953del , CM000669.2:g.142751953del	GRCh38
NC_000007.13:g.142459804del , CM000669.1:g.142459804del	GRCh37
NC_000007.12:g.142139378del	NCBI36
NG_008307.3:g.7470del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.380del (PRSS1) MANE Select	ENSP00000308720.7:p.Ser127PhefsTer?
ENST00000311737.11:c.380del (PRSS1)	ENSP00000308720.7:p.Ser127PhefsTer?
ENST00000463701.1:n.844del (PRSS1)
ENST00000485223.1:n.1378del (PRSS1)
ENST00000486171.5:c.422del (PRSS1)	ENSP00000417854.1:p.Ser141PhefsTer?
ENST00000492062.1:c.230del (PRSS1)	ENSP00000419912.1:p.Ser77PhefsTer?
ENST00000610416.2:c.370+30767del (TRBC1)	ENSP00000482915.1:n.370+30767del
ENST00000612126.4:c.380del (PRSS1)	ENSP00000479959.1:p.Ser127PhefsTer?
ENST00000619214.4:c.350del (PRSS1)	ENSP00000481361.1:p.Ser117PhefsTer?
ENST00000633114.1:c.321+59del (PRSS2)	ENSP00000487822.1:n.321+59del
ENST00000634019.1:c.82+3162del (PRSS2)	ENSP00000488594.1:n.82+3162del
NM_002769.4:c.380del (PRSS1)	NP_002760.1:p.Ser127PhefsTer?
XM_011516411.1:c.1055del (PRSS1)	XP_011514713.1:p.Ser352PhefsTer?
NM_002769.5:c.380del (PRSS1) MANE Select	NP_002760.1:p.Ser127PhefsTer?
NR_172947.1:n.322del (PRSS1)
NR_172948.1:n.319del (PRSS1)
NR_172949.1:n.319del (PRSS1)
NR_172950.1:n.233del (PRSS1)
NR_172951.1:n.167del (PRSS1)