Canonical Allele Identifier: CA645558774

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• gnomAD v4: 7-142750577-TGAC-T
• COSMIC: COSM1733282

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142750578_142750580del , CM000669.2:g.142750578_142750580del	GRCh38
NC_000007.13:g.142458429_142458431del , CM000669.1:g.142458429_142458431del	GRCh37
NC_000007.12:g.142138003_142138005del	NCBI36
NG_008307.3:g.6095_6097del

Transcript Alleles

HGVS	Amino-acid change
ENST00000311737.12:c.64_66del (PRSS1) MANE Select	ENSP00000308720.7:p.Asp22del
ENST00000311737.11:c.64_66del (PRSS1)	ENSP00000308720.7:p.Asp22del
ENST00000485223.1:n.54-51_54-49del (PRSS1)
ENST00000486171.5:c.64_66del (PRSS1)	ENSP00000417854.1:p.Asp22del
ENST00000497041.1:n.68_70del (PRSS1)
ENST00000610416.2:c.370+29392_370+29394del (TRBC1)	ENSP00000482915.1:n.370+29392_370+29394de...
ENST00000612126.4:c.64_66del (PRSS1)	ENSP00000479959.1:p.Asp22del
ENST00000619214.4:c.64_66del (PRSS1)	ENSP00000481361.1:p.Asp22del
ENST00000633114.1:c.64_66del (PRSS2)	ENSP00000487822.1:p.Asp22del
ENST00000634019.1:c.82+1787_82+1789del (PRSS2)	ENSP00000488594.1:n.82+1787_82+1789del
NM_002769.4:c.64_66del (PRSS1)	NP_002760.1:p.Asp22del
XM_011516411.1:c.739_741del (PRSS1)	XP_011514713.1:p.Asp247del
NM_002769.5:c.64_66del (PRSS1) MANE Select	NP_002760.1:p.Asp22del
NR_172947.1:n.77_79del (PRSS1)
NR_172948.1:n.77_79del (PRSS1)
NR_172949.1:n.54-51_54-49del (PRSS1)
NR_172950.1:n.53+1054_53+1056del (PRSS1)
NR_172951.1:n.54-51_54-49del (PRSS1)