Canonical Allele Identifier: CA1108079769

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• gnomAD v3: 7-142752237-T-TGCC
• gnomAD v4: 7-142752237-T-TGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752237_142752238insGCC , CM000669.2:g.142752237_142752238insGCC	GRCh38
NC_000007.13:g.142460088_142460089insGCC , CM000669.1:g.142460088_142460089insGCC	GRCh37
NC_000007.12:g.142139662_142139663insGCC	NCBI36
NG_008307.3:g.7754_7755insGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.455-194_455-193insGCC (PRSS1) MANE Select	ENSP00000308720.7:n.455-194_455-193insGCC
ENST00000311737.11:c.455-194_455-193insGCC (PRSS1)	ENSP00000308720.7:n.455-194_455-193insGCC
ENST00000463701.1:n.919-194_919-193insGCC (PRSS1)
ENST00000486171.5:c.497-194_497-193insGCC (PRSS1)	ENSP00000417854.1:n.497-194_497-193insGCC
ENST00000492062.1:c.305-194_305-193insGCC (PRSS1)	ENSP00000419912.1:n.305-194_305-193insGCC
ENST00000610416.2:c.370+31051_370+31052insGCC (TRBC1)	ENSP00000482915.1:n.370+31051_370+31052insGCC
ENST00000612126.4:c.455-194_455-193insGCC (PRSS1)	ENSP00000479959.1:n.455-194_455-193insGCC
ENST00000619214.4:c.425-194_425-193insGCC (PRSS1)	ENSP00000481361.1:n.425-194_425-193insGCC
ENST00000633114.1:c.321+343_321+344insGCC (PRSS2)	ENSP00000487822.1:n.321+343_321+344insGCC
ENST00000634019.1:c.82+3446_82+3447insGCC (PRSS2)	ENSP00000488594.1:n.82+3446_82+3447insGCC
NM_002769.4:c.455-194_455-193insGCC (PRSS1)	NP_002760.1:n.455-194_455-193insGCC
XM_011516411.1:c.1130-194_1130-193insGCC (PRSS1)	XP_011514713.1:n.1130-194_1130-193insGCC
NM_002769.5:c.455-194_455-193insGCC (PRSS1) MANE Select	NP_002760.1:n.455-194_455-193insGCC
NR_172947.1:n.397-194_397-193insGCC (PRSS1)
NR_172948.1:n.394-194_394-193insGCC (PRSS1)
NR_172949.1:n.394-194_394-193insGCC (PRSS1)
NR_172950.1:n.308-194_308-193insGCC (PRSS1)
NR_172951.1:n.242-194_242-193insGCC (PRSS1)