Canonical Allele Identifier: CA369609244

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• MyVariant Identifiers: chr7:g.142459870G>C (hg19) ; chr7:g.142752019G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752019G>C , CM000669.2:g.142752019G>C	GRCh38
NC_000007.13:g.142459870G>C , CM000669.1:g.142459870G>C	GRCh37
NC_000007.12:g.142139444G>C	NCBI36
NG_008307.3:g.7536G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.446G>C (PRSS1) MANE Select	ENSP00000308720.7:p.Ser149Thr
ENST00000311737.11:c.446G>C (PRSS1)	ENSP00000308720.7:p.Ser149Thr
ENST00000463701.1:n.910G>C (PRSS1)
ENST00000486171.5:c.488G>C (PRSS1)	ENSP00000417854.1:p.Ser163Thr
ENST00000492062.1:c.296G>C (PRSS1)	ENSP00000419912.1:p.Ser99Thr
ENST00000610416.2:c.370+30833G>C (TRBC1)	ENSP00000482915.1:n.370+30833G>C
ENST00000612126.4:c.446G>C (PRSS1)	ENSP00000479959.1:p.Ser149Thr
ENST00000619214.4:c.416G>C (PRSS1)	ENSP00000481361.1:p.Ser139Thr
ENST00000633114.1:c.321+125G>C (PRSS2)	ENSP00000487822.1:n.321+125G>C
ENST00000634019.1:c.82+3228G>C (PRSS2)	ENSP00000488594.1:n.82+3228G>C
NM_002769.4:c.446G>C (PRSS1)	NP_002760.1:p.Ser149Thr
XM_011516411.1:c.1121G>C (PRSS1)	XP_011514713.1:p.Ser374Thr
NM_002769.5:c.446G>C (PRSS1) MANE Select	NP_002760.1:p.Ser149Thr
NR_172947.1:n.388G>C (PRSS1)
NR_172948.1:n.385G>C (PRSS1)
NR_172949.1:n.385G>C (PRSS1)
NR_172950.1:n.299G>C (PRSS1)
NR_172951.1:n.233G>C (PRSS1)