Canonical Allele Identifier: CA2685350248

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• gnomAD v4: 7-142752353-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752354_142752355del , CM000669.2:g.142752354_142752355del	GRCh38
NC_000007.13:g.142460205_142460206del , CM000669.1:g.142460205_142460206del	GRCh37
NC_000007.12:g.142139779_142139780del	NCBI36
NG_008307.3:g.7871_7872del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.455-77_455-76del (PRSS1) MANE Select	ENSP00000308720.7:n.455-77_455-76del
ENST00000311737.11:c.455-77_455-76del (PRSS1)	ENSP00000308720.7:n.455-77_455-76del
ENST00000463701.1:n.919-77_919-76del (PRSS1)
ENST00000486171.5:c.497-77_497-76del (PRSS1)	ENSP00000417854.1:n.497-77_497-76del
ENST00000492062.1:c.305-77_305-76del (PRSS1)	ENSP00000419912.1:n.305-77_305-76del
ENST00000610416.2:c.370+31168_370+31169del (TRBC1)	ENSP00000482915.1:n.370+31168_370+31169del
ENST00000612126.4:c.455-77_455-76del (PRSS1)	ENSP00000479959.1:n.455-77_455-76del
ENST00000619214.4:c.425-77_425-76del (PRSS1)	ENSP00000481361.1:n.425-77_425-76del
ENST00000633114.1:c.321+460_321+461del (PRSS2)	ENSP00000487822.1:n.321+460_321+461del
ENST00000634019.1:c.82+3563_82+3564del (PRSS2)	ENSP00000488594.1:n.82+3563_82+3564del
NM_002769.4:c.455-77_455-76del (PRSS1)	NP_002760.1:n.455-77_455-76del
XM_011516411.1:c.1130-77_1130-76del (PRSS1)	XP_011514713.1:n.1130-77_1130-76del
NM_002769.5:c.455-77_455-76del (PRSS1) MANE Select	NP_002760.1:n.455-77_455-76del
NR_172947.1:n.397-77_397-76del (PRSS1)
NR_172948.1:n.394-77_394-76del (PRSS1)
NR_172949.1:n.394-77_394-76del (PRSS1)
NR_172950.1:n.308-77_308-76del (PRSS1)
NR_172951.1:n.242-77_242-76del (PRSS1)