Canonical Allele Identifier: CA2685349978

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• gnomAD v4: 7-142752314-T-TCC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752314_142752315insCC , CM000669.2:g.142752314_142752315insCC	GRCh38
NC_000007.13:g.142460165_142460166insCC , CM000669.1:g.142460165_142460166insCC	GRCh37
NC_000007.12:g.142139739_142139740insCC	NCBI36
NG_008307.3:g.7831_7832insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.455-117_455-116insCC (PRSS1) MANE Select	ENSP00000308720.7:n.455-117_455-116insCC
ENST00000311737.11:c.455-117_455-116insCC (PRSS1)	ENSP00000308720.7:n.455-117_455-116insCC
ENST00000463701.1:n.919-117_919-116insCC (PRSS1)
ENST00000486171.5:c.497-117_497-116insCC (PRSS1)	ENSP00000417854.1:n.497-117_497-116insCC
ENST00000492062.1:c.305-117_305-116insCC (PRSS1)	ENSP00000419912.1:n.305-117_305-116insCC
ENST00000610416.2:c.370+31128_370+31129insCC (TRBC1)	ENSP00000482915.1:n.370+31128_370+31129insCC
ENST00000612126.4:c.455-117_455-116insCC (PRSS1)	ENSP00000479959.1:n.455-117_455-116insCC
ENST00000619214.4:c.425-117_425-116insCC (PRSS1)	ENSP00000481361.1:n.425-117_425-116insCC
ENST00000633114.1:c.321+420_321+421insCC (PRSS2)	ENSP00000487822.1:n.321+420_321+421insCC
ENST00000634019.1:c.82+3523_82+3524insCC (PRSS2)	ENSP00000488594.1:n.82+3523_82+3524insCC
NM_002769.4:c.455-117_455-116insCC (PRSS1)	NP_002760.1:n.455-117_455-116insCC
XM_011516411.1:c.1130-117_1130-116insCC (PRSS1)	XP_011514713.1:n.1130-117_1130-116insCC
NM_002769.5:c.455-117_455-116insCC (PRSS1) MANE Select	NP_002760.1:n.455-117_455-116insCC
NR_172947.1:n.397-117_397-116insCC (PRSS1)
NR_172948.1:n.394-117_394-116insCC (PRSS1)
NR_172949.1:n.394-117_394-116insCC (PRSS1)
NR_172950.1:n.308-117_308-116insCC (PRSS1)
NR_172951.1:n.242-117_242-116insCC (PRSS1)