Canonical Allele Identifier: CA2685349362

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• gnomAD v4: 7-142752082-AAACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752084_142752087del , CM000669.2:g.142752084_142752087del	GRCh38
NC_000007.13:g.142459935_142459938del , CM000669.1:g.142459935_142459938del	GRCh37
NC_000007.12:g.142139509_142139512del	NCBI36
NG_008307.3:g.7601_7604del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.454+57_454+60del (PRSS1) MANE Select	ENSP00000308720.7:n.454+57_454+60del
ENST00000311737.11:c.454+57_454+60del (PRSS1)	ENSP00000308720.7:n.454+57_454+60del
ENST00000463701.1:n.918+57_918+60del (PRSS1)
ENST00000486171.5:c.496+57_496+60del (PRSS1)	ENSP00000417854.1:n.496+57_496+60del
ENST00000492062.1:c.304+57_304+60del (PRSS1)	ENSP00000419912.1:n.304+57_304+60del
ENST00000610416.2:c.370+30898_370+30901del (TRBC1)	ENSP00000482915.1:n.370+30898_370+30901del
ENST00000612126.4:c.454+57_454+60del (PRSS1)	ENSP00000479959.1:n.454+57_454+60del
ENST00000619214.4:c.424+57_424+60del (PRSS1)	ENSP00000481361.1:n.424+57_424+60del
ENST00000633114.1:c.321+190_321+193del (PRSS2)	ENSP00000487822.1:n.321+190_321+193del
ENST00000634019.1:c.82+3293_82+3296del (PRSS2)	ENSP00000488594.1:n.82+3293_82+3296del
NM_002769.4:c.454+57_454+60del (PRSS1)	NP_002760.1:n.454+57_454+60del
XM_011516411.1:c.1129+57_1129+60del (PRSS1)	XP_011514713.1:n.1129+57_1129+60del
NM_002769.5:c.454+57_454+60del (PRSS1) MANE Select	NP_002760.1:n.454+57_454+60del
NR_172947.1:n.396+57_396+60del (PRSS1)
NR_172948.1:n.393+57_393+60del (PRSS1)
NR_172949.1:n.393+57_393+60del (PRSS1)
NR_172950.1:n.307+57_307+60del (PRSS1)
NR_172951.1:n.241+57_241+60del (PRSS1)