Canonical Allele Identifier: CA458538324

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• MyVariant Identifiers: chr7:g.142459823A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751972A>G , CM000669.2:g.142751972A>G	GRCh38
NC_000007.13:g.142459823A>G , CM000669.1:g.142459823A>G	GRCh37
NC_000007.12:g.142139397A>G	NCBI36
NG_008307.3:g.7489A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.399A>G (PRSS1) MANE Select	ENSP00000308720.7:p.Pro133=
ENST00000311737.11:c.399A>G (PRSS1)	ENSP00000308720.7:p.Pro133=
ENST00000463701.1:n.863A>G (PRSS1)
ENST00000485223.1:n.1397A>G (PRSS1)
ENST00000486171.5:c.441A>G (PRSS1)	ENSP00000417854.1:p.Pro147=
ENST00000492062.1:c.249A>G (PRSS1)	ENSP00000419912.1:p.Pro83=
ENST00000610416.2:c.370+30786A>G (TRBC1)	ENSP00000482915.1:n.370+30786A>G
ENST00000612126.4:c.399A>G (PRSS1)	ENSP00000479959.1:p.Pro133=
ENST00000619214.4:c.369A>G (PRSS1)	ENSP00000481361.1:p.Pro123=
ENST00000633114.1:c.321+78A>G (PRSS2)	ENSP00000487822.1:n.321+78A>G
ENST00000634019.1:c.82+3181A>G (PRSS2)	ENSP00000488594.1:n.82+3181A>G
NM_002769.4:c.399A>G (PRSS1)	NP_002760.1:p.Pro133=
XM_011516411.1:c.1074A>G (PRSS1)	XP_011514713.1:p.Pro358=
NM_002769.5:c.399A>G (PRSS1) MANE Select	NP_002760.1:p.Pro133=
NR_172947.1:n.341A>G (PRSS1)
NR_172948.1:n.338A>G (PRSS1)
NR_172949.1:n.338A>G (PRSS1)
NR_172950.1:n.252A>G (PRSS1)
NR_172951.1:n.186A>G (PRSS1)