Canonical Allele Identifier: CA369608754

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• MyVariant Identifiers: chr7:g.142459731A>C (hg19) ; chr7:g.142751880A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751880A>C , CM000669.2:g.142751880A>C	GRCh38
NC_000007.13:g.142459731A>C , CM000669.1:g.142459731A>C	GRCh37
NC_000007.12:g.142139305A>C	NCBI36
NG_008307.3:g.7397A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.307A>C (PRSS1) MANE Select	ENSP00000308720.7:p.Thr103Pro
ENST00000311737.11:c.307A>C (PRSS1)	ENSP00000308720.7:p.Thr103Pro
ENST00000463701.1:n.771A>C (PRSS1)
ENST00000485223.1:n.1305A>C (PRSS1)
ENST00000486171.5:c.349A>C (PRSS1)	ENSP00000417854.1:p.Thr117Pro
ENST00000492062.1:c.157A>C (PRSS1)	ENSP00000419912.1:p.Thr53Pro
ENST00000610416.2:c.370+30694A>C (TRBC1)	ENSP00000482915.1:n.370+30694A>C
ENST00000612126.4:c.307A>C (PRSS1)	ENSP00000479959.1:p.Thr103Pro
ENST00000619214.4:c.277A>C (PRSS1)	ENSP00000481361.1:p.Thr93Pro
ENST00000633114.1:c.307A>C (PRSS2)	ENSP00000487822.1:p.Thr103Pro
ENST00000634019.1:c.82+3089A>C (PRSS2)	ENSP00000488594.1:n.82+3089A>C
NM_002769.4:c.307A>C (PRSS1)	NP_002760.1:p.Thr103Pro
XM_011516411.1:c.982A>C (PRSS1)	XP_011514713.1:p.Thr328Pro
NM_002769.5:c.307A>C (PRSS1) MANE Select	NP_002760.1:p.Thr103Pro
NR_172947.1:n.249A>C (PRSS1)
NR_172948.1:n.246A>C (PRSS1)
NR_172949.1:n.246A>C (PRSS1)
NR_172950.1:n.160A>C (PRSS1)
NR_172951.1:n.140-46A>C (PRSS1)