Canonical Allele Identifier: CA1748624720

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142753050C= , CM000669.2:g.142753050C=	GRCh38
NC_000007.13:g.142460901C= , CM000669.1:g.142460901C=	GRCh37
NC_000007.12:g.142140475C=	NCBI36
NG_008307.3:g.8567C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000311737.12:c.*30C= (PRSS1) MANE Select	ENSP00000308720.7:n.*30C=
ENST00000311737.11:c.*30C= (PRSS1)	ENSP00000308720.7:n.*30C=
ENST00000463701.1:n.1238C= (PRSS1)
ENST00000492062.1:c.607C= (PRSS1)	ENSP00000419912.1:n.607C=
ENST00000610416.2:c.370+31864C= (TRBC1)	ENSP00000482915.1:n.370+31864C=
ENST00000612126.4:c.591+483C= (PRSS1)	ENSP00000479959.1:n.591+483C=
ENST00000619214.4:c.*30C= (PRSS1)	ENSP00000481361.1:n.*30C=
ENST00000633114.1:c.321+1156C= (PRSS2)	ENSP00000487822.1:n.321+1156C=
ENST00000634019.1:c.82+4259C= (PRSS2)	ENSP00000488594.1:n.82+4259C=
NM_002769.4:c.*30C= (PRSS1)	NP_002760.1:n.*30C=
XM_011516411.1:c.*30C= (PRSS1)	XP_011514713.1:n.*30C=
NM_002769.5:c.*30C= (PRSS1) MANE Select	NP_002760.1:n.*30C=
NR_172947.1:n.716C= (PRSS1)
NR_172948.1:n.713C= (PRSS1)
NR_172949.1:n.713C= (PRSS1)
NR_172950.1:n.627C= (PRSS1)
NR_172951.1:n.561C= (PRSS1)