Canonical Allele Identifier: CA2579047824

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751790del , CM000669.2:g.142751790del	GRCh38
NC_000007.13:g.142459641del , CM000669.1:g.142459641del	GRCh37
NC_000007.12:g.142139215del	NCBI36
NG_008307.3:g.7307del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.217del (PRSS1) MANE Select	ENSP00000308720.7:p.Leu73TrpfsTer?
ENST00000311737.11:c.217del (PRSS1)	ENSP00000308720.7:p.Leu73TrpfsTer?
ENST00000463701.1:n.681del (PRSS1)
ENST00000485223.1:n.1215del (PRSS1)
ENST00000486171.5:c.259del (PRSS1)	ENSP00000417854.1:p.Leu87TrpfsTer?
ENST00000492062.1:c.67del (PRSS1)	ENSP00000419912.1:p.Leu23TrpfsTer?
ENST00000610416.2:c.370+30604del (TRBC1)	ENSP00000482915.1:n.370+30604del
ENST00000612126.4:c.217del (PRSS1)	ENSP00000479959.1:p.Leu73TrpfsTer?
ENST00000619214.4:c.217del (PRSS1)	ENSP00000481361.1:p.Leu73TrpfsTer22
ENST00000633114.1:c.217del (PRSS2)	ENSP00000487822.1:p.Leu73TrpfsTer?
ENST00000634019.1:c.82+2999del (PRSS2)	ENSP00000488594.1:n.82+2999del
NM_002769.4:c.217del (PRSS1)	NP_002760.1:p.Leu73TrpfsTer?
XM_011516411.1:c.892del (PRSS1)	XP_011514713.1:p.Leu298TrpfsTer?
NM_002769.5:c.217del (PRSS1) MANE Select	NP_002760.1:p.Leu73TrpfsTer?
NR_172947.1:n.198-39del (PRSS1)
NR_172948.1:n.198-42del (PRSS1)
NR_172949.1:n.156del (PRSS1)
NR_172950.1:n.70del (PRSS1)
NR_172951.1:n.140-136del (PRSS1)