Canonical Allele Identifier: CA2778215850

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752244_142752247del , CM000669.2:g.142752244_142752247del	GRCh38
NC_000007.13:g.142460095_142460098del , CM000669.1:g.142460095_142460098del	GRCh37
NC_000007.12:g.142139669_142139672del	NCBI36
NG_008307.3:g.7761_7764del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.455-187_455-184del (PRSS1) MANE Select	ENSP00000308720.7:n.455-187_455-184del
ENST00000311737.11:c.455-187_455-184del (PRSS1)	ENSP00000308720.7:n.455-187_455-184del
ENST00000463701.1:n.919-187_919-184del (PRSS1)
ENST00000486171.5:c.497-187_497-184del (PRSS1)	ENSP00000417854.1:n.497-187_497-184del
ENST00000492062.1:c.305-187_305-184del (PRSS1)	ENSP00000419912.1:n.305-187_305-184del
ENST00000610416.2:c.370+31058_370+31061del (TRBC1)	ENSP00000482915.1:n.370+31058_370+31061del
ENST00000612126.4:c.455-187_455-184del (PRSS1)	ENSP00000479959.1:n.455-187_455-184del
ENST00000619214.4:c.425-187_425-184del (PRSS1)	ENSP00000481361.1:n.425-187_425-184del
ENST00000633114.1:c.321+350_321+353del (PRSS2)	ENSP00000487822.1:n.321+350_321+353del
ENST00000634019.1:c.82+3453_82+3456del (PRSS2)	ENSP00000488594.1:n.82+3453_82+3456del
NM_002769.4:c.455-187_455-184del (PRSS1)	NP_002760.1:n.455-187_455-184del
XM_011516411.1:c.1130-187_1130-184del (PRSS1)	XP_011514713.1:n.1130-187_1130-184del
NM_002769.5:c.455-187_455-184del (PRSS1) MANE Select	NP_002760.1:n.455-187_455-184del
NR_172947.1:n.397-187_397-184del (PRSS1)
NR_172948.1:n.394-187_394-184del (PRSS1)
NR_172949.1:n.394-187_394-184del (PRSS1)
NR_172950.1:n.308-187_308-184del (PRSS1)
NR_172951.1:n.242-187_242-184del (PRSS1)