Canonical Allele Identifier: CA1108080034

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• gnomAD v3: 7-142752349-A-AAG
• gnomAD v4: 7-142752349-A-AAG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752349_142752350insAG , CM000669.2:g.142752349_142752350insAG	GRCh38
NC_000007.13:g.142460200_142460201insAG , CM000669.1:g.142460200_142460201insAG	GRCh37
NC_000007.12:g.142139774_142139775insAG	NCBI36
NG_008307.3:g.7866_7867insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.455-82_455-81insAG (PRSS1) MANE Select	ENSP00000308720.7:n.455-82_455-81insAG
ENST00000311737.11:c.455-82_455-81insAG (PRSS1)	ENSP00000308720.7:n.455-82_455-81insAG
ENST00000463701.1:n.919-82_919-81insAG (PRSS1)
ENST00000486171.5:c.497-82_497-81insAG (PRSS1)	ENSP00000417854.1:n.497-82_497-81insAG
ENST00000492062.1:c.305-82_305-81insAG (PRSS1)	ENSP00000419912.1:n.305-82_305-81insAG
ENST00000610416.2:c.370+31163_370+31164insAG (TRBC1)	ENSP00000482915.1:n.370+31163_370+31164insAG
ENST00000612126.4:c.455-82_455-81insAG (PRSS1)	ENSP00000479959.1:n.455-82_455-81insAG
ENST00000619214.4:c.425-82_425-81insAG (PRSS1)	ENSP00000481361.1:n.425-82_425-81insAG
ENST00000633114.1:c.321+455_321+456insAG (PRSS2)	ENSP00000487822.1:n.321+455_321+456insAG
ENST00000634019.1:c.82+3558_82+3559insAG (PRSS2)	ENSP00000488594.1:n.82+3558_82+3559insAG
NM_002769.4:c.455-82_455-81insAG (PRSS1)	NP_002760.1:n.455-82_455-81insAG
XM_011516411.1:c.1130-82_1130-81insAG (PRSS1)	XP_011514713.1:n.1130-82_1130-81insAG
NM_002769.5:c.455-82_455-81insAG (PRSS1) MANE Select	NP_002760.1:n.455-82_455-81insAG
NR_172947.1:n.397-82_397-81insAG (PRSS1)
NR_172948.1:n.394-82_394-81insAG (PRSS1)
NR_172949.1:n.394-82_394-81insAG (PRSS1)
NR_172950.1:n.308-82_308-81insAG (PRSS1)
NR_172951.1:n.242-82_242-81insAG (PRSS1)