Canonical Allele Identifier: CA168149078

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• dbSNP Id: rs753133399
• gnomAD v4: 7-142752290-CAG-C
• MyVariant Identifiers: chr7:g.142460142_142460143del (hg19) ; chr7:g.142752291_142752292del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752293_142752294del , CM000669.2:g.142752293_142752294del	GRCh38
NC_000007.13:g.142460144_142460145del , CM000669.1:g.142460144_142460145del	GRCh37
NC_000007.12:g.142139718_142139719del	NCBI36
NG_008307.3:g.7810_7811del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.455-138_455-137del (PRSS1) MANE Select	ENSP00000308720.7:n.455-138_455-137del
ENST00000311737.11:c.455-138_455-137del (PRSS1)	ENSP00000308720.7:n.455-138_455-137del
ENST00000463701.1:n.919-138_919-137del (PRSS1)
ENST00000486171.5:c.497-138_497-137del (PRSS1)	ENSP00000417854.1:n.497-138_497-137del
ENST00000492062.1:c.305-138_305-137del (PRSS1)	ENSP00000419912.1:n.305-138_305-137del
ENST00000610416.2:c.370+31107_370+31108del (TRBC1)	ENSP00000482915.1:n.370+31107_370+31108del
ENST00000612126.4:c.455-138_455-137del (PRSS1)	ENSP00000479959.1:n.455-138_455-137del
ENST00000619214.4:c.425-138_425-137del (PRSS1)	ENSP00000481361.1:n.425-138_425-137del
ENST00000633114.1:c.321+399_321+400del (PRSS2)	ENSP00000487822.1:n.321+399_321+400del
ENST00000634019.1:c.82+3502_82+3503del (PRSS2)	ENSP00000488594.1:n.82+3502_82+3503del
NM_002769.4:c.455-138_455-137del (PRSS1)	NP_002760.1:n.455-138_455-137del
XM_011516411.1:c.1130-138_1130-137del (PRSS1)	XP_011514713.1:n.1130-138_1130-137del
NM_002769.5:c.455-138_455-137del (PRSS1) MANE Select	NP_002760.1:n.455-138_455-137del
NR_172947.1:n.397-138_397-137del (PRSS1)
NR_172948.1:n.394-138_394-137del (PRSS1)
NR_172949.1:n.394-138_394-137del (PRSS1)
NR_172950.1:n.308-138_308-137del (PRSS1)
NR_172951.1:n.242-138_242-137del (PRSS1)