Canonical Allele Identifier: CA1748623630

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751978T= , CM000669.2:g.142751978T=	GRCh38
NC_000007.13:g.142459829T= , CM000669.1:g.142459829T=	GRCh37
NC_000007.12:g.142139403T=	NCBI36
NG_008307.3:g.7495T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.405T= (PRSS1) MANE Select	ENSP00000308720.7:p.Thr135=
ENST00000311737.11:c.405T= (PRSS1)	ENSP00000308720.7:p.Thr135=
ENST00000463701.1:n.869T= (PRSS1)
ENST00000485223.1:n.1403T= (PRSS1)
ENST00000486171.5:c.447T= (PRSS1)	ENSP00000417854.1:p.Thr149=
ENST00000492062.1:c.255T= (PRSS1)	ENSP00000419912.1:p.Thr85=
ENST00000610416.2:c.370+30792T= (TRBC1)	ENSP00000482915.1:n.370+30792T=
ENST00000612126.4:c.405T= (PRSS1)	ENSP00000479959.1:p.Thr135=
ENST00000619214.4:c.375T= (PRSS1)	ENSP00000481361.1:p.Thr125=
ENST00000633114.1:c.321+84T= (PRSS2)	ENSP00000487822.1:n.321+84T=
ENST00000634019.1:c.82+3187T= (PRSS2)	ENSP00000488594.1:n.82+3187T=
NM_002769.4:c.405T= (PRSS1)	NP_002760.1:p.Thr135=
XM_011516411.1:c.1080T= (PRSS1)	XP_011514713.1:p.Thr360=
NM_002769.5:c.405T= (PRSS1) MANE Select	NP_002760.1:p.Thr135=
NR_172947.1:n.347T= (PRSS1)
NR_172948.1:n.344T= (PRSS1)
NR_172949.1:n.344T= (PRSS1)
NR_172950.1:n.258T= (PRSS1)
NR_172951.1:n.192T= (PRSS1)