Canonical Allele Identifier: CA2685349947

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• gnomAD v4: 7-142752310-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752311del , CM000669.2:g.142752311del	GRCh38
NC_000007.13:g.142460162del , CM000669.1:g.142460162del	GRCh37
NC_000007.12:g.142139736del	NCBI36
NG_008307.3:g.7828del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.455-120del (PRSS1) MANE Select	ENSP00000308720.7:n.455-120del
ENST00000311737.11:c.455-120del (PRSS1)	ENSP00000308720.7:n.455-120del
ENST00000463701.1:n.919-120del (PRSS1)
ENST00000486171.5:c.497-120del (PRSS1)	ENSP00000417854.1:n.497-120del
ENST00000492062.1:c.305-120del (PRSS1)	ENSP00000419912.1:n.305-120del
ENST00000610416.2:c.370+31125del (TRBC1)	ENSP00000482915.1:n.370+31125del
ENST00000612126.4:c.455-120del (PRSS1)	ENSP00000479959.1:n.455-120del
ENST00000619214.4:c.425-120del (PRSS1)	ENSP00000481361.1:n.425-120del
ENST00000633114.1:c.321+417del (PRSS2)	ENSP00000487822.1:n.321+417del
ENST00000634019.1:c.82+3520del (PRSS2)	ENSP00000488594.1:n.82+3520del
NM_002769.4:c.455-120del (PRSS1)	NP_002760.1:n.455-120del
XM_011516411.1:c.1130-120del (PRSS1)	XP_011514713.1:n.1130-120del
NM_002769.5:c.455-120del (PRSS1) MANE Select	NP_002760.1:n.455-120del
NR_172947.1:n.397-120del (PRSS1)
NR_172948.1:n.394-120del (PRSS1)
NR_172949.1:n.394-120del (PRSS1)
NR_172950.1:n.308-120del (PRSS1)
NR_172951.1:n.242-120del (PRSS1)