Canonical Allele Identifier: CA1108079765

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• dbSNP Id: rs2116981440
• gnomAD v3: 7-142752235-GAT-G
• gnomAD v4: 7-142752235-GAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752238_142752239del , CM000669.2:g.142752238_142752239del	GRCh38
NC_000007.13:g.142460089_142460090del , CM000669.1:g.142460089_142460090del	GRCh37
NC_000007.12:g.142139663_142139664del	NCBI36
NG_008307.3:g.7755_7756del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.455-193_455-192del (PRSS1) MANE Select	ENSP00000308720.7:n.455-193_455-192del
ENST00000311737.11:c.455-193_455-192del (PRSS1)	ENSP00000308720.7:n.455-193_455-192del
ENST00000463701.1:n.919-193_919-192del (PRSS1)
ENST00000486171.5:c.497-193_497-192del (PRSS1)	ENSP00000417854.1:n.497-193_497-192del
ENST00000492062.1:c.305-193_305-192del (PRSS1)	ENSP00000419912.1:n.305-193_305-192del
ENST00000610416.2:c.370+31052_370+31053del (TRBC1)	ENSP00000482915.1:n.370+31052_370+31053del
ENST00000612126.4:c.455-193_455-192del (PRSS1)	ENSP00000479959.1:n.455-193_455-192del
ENST00000619214.4:c.425-193_425-192del (PRSS1)	ENSP00000481361.1:n.425-193_425-192del
ENST00000633114.1:c.321+344_321+345del (PRSS2)	ENSP00000487822.1:n.321+344_321+345del
ENST00000634019.1:c.82+3447_82+3448del (PRSS2)	ENSP00000488594.1:n.82+3447_82+3448del
NM_002769.4:c.455-193_455-192del (PRSS1)	NP_002760.1:n.455-193_455-192del
XM_011516411.1:c.1130-193_1130-192del (PRSS1)	XP_011514713.1:n.1130-193_1130-192del
NM_002769.5:c.455-193_455-192del (PRSS1) MANE Select	NP_002760.1:n.455-193_455-192del
NR_172947.1:n.397-193_397-192del (PRSS1)
NR_172948.1:n.394-193_394-192del (PRSS1)
NR_172949.1:n.394-193_394-192del (PRSS1)
NR_172950.1:n.308-193_308-192del (PRSS1)
NR_172951.1:n.242-193_242-192del (PRSS1)