Canonical Allele Identifier: CA2685349114

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• gnomAD v4: 7-142752032-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752032_142752033insC , CM000669.2:g.142752032_142752033insC	GRCh38
NC_000007.13:g.142459883_142459884insC , CM000669.1:g.142459883_142459884insC	GRCh37
NC_000007.12:g.142139457_142139458insC	NCBI36
NG_008307.3:g.7549_7550insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.454+5_454+6insC (PRSS1) MANE Select	ENSP00000308720.7:n.454+5_454+6insC
ENST00000311737.11:c.454+5_454+6insC (PRSS1)	ENSP00000308720.7:n.454+5_454+6insC
ENST00000463701.1:n.918+5_918+6insC (PRSS1)
ENST00000486171.5:c.496+5_496+6insC (PRSS1)	ENSP00000417854.1:n.496+5_496+6insC
ENST00000492062.1:c.304+5_304+6insC (PRSS1)	ENSP00000419912.1:n.304+5_304+6insC
ENST00000610416.2:c.370+30846_370+30847insC (TRBC1)	ENSP00000482915.1:n.370+30846_370+30847insC
ENST00000612126.4:c.454+5_454+6insC (PRSS1)	ENSP00000479959.1:n.454+5_454+6insC
ENST00000619214.4:c.424+5_424+6insC (PRSS1)	ENSP00000481361.1:n.424+5_424+6insC
ENST00000633114.1:c.321+138_321+139insC (PRSS2)	ENSP00000487822.1:n.321+138_321+139insC
ENST00000634019.1:c.82+3241_82+3242insC (PRSS2)	ENSP00000488594.1:n.82+3241_82+3242insC
NM_002769.4:c.454+5_454+6insC (PRSS1)	NP_002760.1:n.454+5_454+6insC
XM_011516411.1:c.1129+5_1129+6insC (PRSS1)	XP_011514713.1:n.1129+5_1129+6insC
NM_002769.5:c.454+5_454+6insC (PRSS1) MANE Select	NP_002760.1:n.454+5_454+6insC
NR_172947.1:n.396+5_396+6insC (PRSS1)
NR_172948.1:n.393+5_393+6insC (PRSS1)
NR_172949.1:n.393+5_393+6insC (PRSS1)
NR_172950.1:n.307+5_307+6insC (PRSS1)
NR_172951.1:n.241+5_241+6insC (PRSS1)