Canonical Allele Identifier: CA1748622219

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142749724_142749725delinsTG , CM000669.2:g.142749724_142749725delinsTG	GRCh38
NC_000007.13:g.142457575_142457576delinsTG , CM000669.1:g.142457575_142457576delinsTG	GRCh37
NC_000007.12:g.142137149_142137150delinsTG	NCBI36
NG_008307.3:g.5241_5242delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000311737.12:c.40+200_40+201delinsTG (PRSS1) MANE Select	ENSP00000308720.7:n.40+200_40+201delinsTG
ENST00000311737.11:c.40+200_40+201delinsTG (PRSS1)	ENSP00000308720.7:n.40+200_40+201delinsTG
ENST00000485223.1:n.53+200_53+201delinsTG (PRSS1)
ENST00000486171.5:c.40+200_40+201delinsTG (PRSS1)	ENSP00000417854.1:n.40+200_40+201delinsTG
ENST00000497041.1:n.44+200_44+201delinsTG (PRSS1)
ENST00000610416.2:c.370+28538_370+28539delinsTG (TRBC1)	ENSP00000482915.1:n.370+28538_370+28539delinsTG
ENST00000612126.4:c.40+200_40+201delinsTG (PRSS1)	ENSP00000479959.1:n.40+200_40+201delinsTG
ENST00000619214.4:c.40+200_40+201delinsTG (PRSS1)	ENSP00000481361.1:n.40+200_40+201delinsTG
ENST00000633114.1:c.40+200_40+201delinsTG (PRSS2)	ENSP00000487822.1:n.40+200_40+201delinsTG
ENST00000634019.1:c.82+933_82+934delinsTG (PRSS2)	ENSP00000488594.1:n.82+933_82+934delinsTG
NM_002769.4:c.40+200_40+201delinsTG (PRSS1)	NP_002760.1:n.40+200_40+201delinsTG
XM_011516411.1:c.715+200_715+201delinsTG (PRSS1)	XP_011514713.1:n.715+200_715+201delinsTG
NM_002769.5:c.40+200_40+201delinsTG (PRSS1) MANE Select	NP_002760.1:n.40+200_40+201delinsTG
NR_172947.1:n.53+200_53+201delinsTG (PRSS1)
NR_172948.1:n.53+200_53+201delinsTG (PRSS1)
NR_172949.1:n.53+200_53+201delinsTG (PRSS1)
NR_172950.1:n.53+200_53+201delinsTG (PRSS1)
NR_172951.1:n.53+200_53+201delinsTG (PRSS1)