Canonical Allele Identifier: CA369608873

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• MyVariant Identifiers: chr7:g.142459768C>G (hg19) ; chr7:g.142751917C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751917C>G , CM000669.2:g.142751917C>G	GRCh38
NC_000007.13:g.142459768C>G , CM000669.1:g.142459768C>G	GRCh37
NC_000007.12:g.142139342C>G	NCBI36
NG_008307.3:g.7434C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.344C>G (PRSS1) MANE Select	ENSP00000308720.7:p.Ser115Ter
ENST00000311737.11:c.344C>G (PRSS1)	ENSP00000308720.7:p.Ser115Ter
ENST00000463701.1:n.808C>G (PRSS1)
ENST00000485223.1:n.1342C>G (PRSS1)
ENST00000486171.5:c.386C>G (PRSS1)	ENSP00000417854.1:p.Ser129Ter
ENST00000492062.1:c.194C>G (PRSS1)	ENSP00000419912.1:p.Ser65Ter
ENST00000610416.2:c.370+30731C>G (TRBC1)	ENSP00000482915.1:n.370+30731C>G
ENST00000612126.4:c.344C>G (PRSS1)	ENSP00000479959.1:p.Ser115Ter
ENST00000619214.4:c.314C>G (PRSS1)	ENSP00000481361.1:p.Ser105Ter
ENST00000633114.1:c.321+23C>G (PRSS2)	ENSP00000487822.1:n.321+23C>G
ENST00000634019.1:c.82+3126C>G (PRSS2)	ENSP00000488594.1:n.82+3126C>G
NM_002769.4:c.344C>G (PRSS1)	NP_002760.1:p.Ser115Ter
XM_011516411.1:c.1019C>G (PRSS1)	XP_011514713.1:p.Ser340Ter
NM_002769.5:c.344C>G (PRSS1) MANE Select	NP_002760.1:p.Ser115Ter
NR_172947.1:n.286C>G (PRSS1)
NR_172948.1:n.283C>G (PRSS1)
NR_172949.1:n.283C>G (PRSS1)
NR_172950.1:n.197C>G (PRSS1)
NR_172951.1:n.140-9C>G (PRSS1)