Canonical Allele Identifier: CA369608914

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• MyVariant Identifiers: chr7:g.142459780T>C (hg19) ; chr7:g.142751929T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751929T>C , CM000669.2:g.142751929T>C	GRCh38
NC_000007.13:g.142459780T>C , CM000669.1:g.142459780T>C	GRCh37
NC_000007.12:g.142139354T>C	NCBI36
NG_008307.3:g.7446T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.356T>C (PRSS1) MANE Select	ENSP00000308720.7:p.Ile119Thr
ENST00000311737.11:c.356T>C (PRSS1)	ENSP00000308720.7:p.Ile119Thr
ENST00000463701.1:n.820T>C (PRSS1)
ENST00000485223.1:n.1354T>C (PRSS1)
ENST00000486171.5:c.398T>C (PRSS1)	ENSP00000417854.1:p.Ile133Thr
ENST00000492062.1:c.206T>C (PRSS1)	ENSP00000419912.1:p.Ile69Thr
ENST00000610416.2:c.370+30743T>C (TRBC1)	ENSP00000482915.1:n.370+30743T>C
ENST00000612126.4:c.356T>C (PRSS1)	ENSP00000479959.1:p.Ile119Thr
ENST00000619214.4:c.326T>C (PRSS1)	ENSP00000481361.1:p.Ile109Thr
ENST00000633114.1:c.321+35T>C (PRSS2)	ENSP00000487822.1:n.321+35T>C
ENST00000634019.1:c.82+3138T>C (PRSS2)	ENSP00000488594.1:n.82+3138T>C
NM_002769.4:c.356T>C (PRSS1)	NP_002760.1:p.Ile119Thr
XM_011516411.1:c.1031T>C (PRSS1)	XP_011514713.1:p.Ile344Thr
NM_002769.5:c.356T>C (PRSS1) MANE Select	NP_002760.1:p.Ile119Thr
NR_172947.1:n.298T>C (PRSS1)
NR_172948.1:n.295T>C (PRSS1)
NR_172949.1:n.295T>C (PRSS1)
NR_172950.1:n.209T>C (PRSS1)
NR_172951.1:n.143T>C (PRSS1)