Canonical Allele Identifier: CA1748622203

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142749695_142749696delinsCA , CM000669.2:g.142749695_142749696delinsCA	GRCh38
NC_000007.13:g.142457546_142457547delinsCA , CM000669.1:g.142457546_142457547delinsCA	GRCh37
NC_000007.12:g.142137120_142137121delinsCA	NCBI36
NG_008307.3:g.5212_5213delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.40+171_40+172delinsCA (PRSS1) MANE Select	ENSP00000308720.7:n.40+171_40+172delinsCA
ENST00000311737.11:c.40+171_40+172delinsCA (PRSS1)	ENSP00000308720.7:n.40+171_40+172delinsCA
ENST00000485223.1:n.53+171_53+172delinsCA (PRSS1)
ENST00000486171.5:c.40+171_40+172delinsCA (PRSS1)	ENSP00000417854.1:n.40+171_40+172delinsCA
ENST00000497041.1:n.44+171_44+172delinsCA (PRSS1)
ENST00000610416.2:c.370+28509_370+28510delinsCA (TRBC1)	ENSP00000482915.1:n.370+28509_370+28510delinsCA
ENST00000612126.4:c.40+171_40+172delinsCA (PRSS1)	ENSP00000479959.1:n.40+171_40+172delinsCA
ENST00000619214.4:c.40+171_40+172delinsCA (PRSS1)	ENSP00000481361.1:n.40+171_40+172delinsCA
ENST00000633114.1:c.40+171_40+172delinsCA (PRSS2)	ENSP00000487822.1:n.40+171_40+172delinsCA
ENST00000634019.1:c.82+904_82+905delinsCA (PRSS2)	ENSP00000488594.1:n.82+904_82+905delinsCA
NM_002769.4:c.40+171_40+172delinsCA (PRSS1)	NP_002760.1:n.40+171_40+172delinsCA
XM_011516411.1:c.715+171_715+172delinsCA (PRSS1)	XP_011514713.1:n.715+171_715+172delinsCA
NM_002769.5:c.40+171_40+172delinsCA (PRSS1) MANE Select	NP_002760.1:n.40+171_40+172delinsCA
NR_172947.1:n.53+171_53+172delinsCA (PRSS1)
NR_172948.1:n.53+171_53+172delinsCA (PRSS1)
NR_172949.1:n.53+171_53+172delinsCA (PRSS1)
NR_172950.1:n.53+171_53+172delinsCA (PRSS1)
NR_172951.1:n.53+171_53+172delinsCA (PRSS1)