Canonical Allele Identifier: CA369609241

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• dbSNP Id: rs1798781513
• MyVariant Identifiers: chr7:g.142459869A>G (hg19) ; chr7:g.142752018A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752018A>G , CM000669.2:g.142752018A>G	GRCh38
NC_000007.13:g.142459869A>G , CM000669.1:g.142459869A>G	GRCh37
NC_000007.12:g.142139443A>G	NCBI36
NG_008307.3:g.7535A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.445A>G (PRSS1) MANE Select	ENSP00000308720.7:p.Ser149Gly
ENST00000311737.11:c.445A>G (PRSS1)	ENSP00000308720.7:p.Ser149Gly
ENST00000463701.1:n.909A>G (PRSS1)
ENST00000486171.5:c.487A>G (PRSS1)	ENSP00000417854.1:p.Ser163Gly
ENST00000492062.1:c.295A>G (PRSS1)	ENSP00000419912.1:p.Ser99Gly
ENST00000610416.2:c.370+30832A>G (TRBC1)	ENSP00000482915.1:n.370+30832A>G
ENST00000612126.4:c.445A>G (PRSS1)	ENSP00000479959.1:p.Ser149Gly
ENST00000619214.4:c.415A>G (PRSS1)	ENSP00000481361.1:p.Ser139Gly
ENST00000633114.1:c.321+124A>G (PRSS2)	ENSP00000487822.1:n.321+124A>G
ENST00000634019.1:c.82+3227A>G (PRSS2)	ENSP00000488594.1:n.82+3227A>G
NM_002769.4:c.445A>G (PRSS1)	NP_002760.1:p.Ser149Gly
XM_011516411.1:c.1120A>G (PRSS1)	XP_011514713.1:p.Ser374Gly
NM_002769.5:c.445A>G (PRSS1) MANE Select	NP_002760.1:p.Ser149Gly
NR_172947.1:n.387A>G (PRSS1)
NR_172948.1:n.384A>G (PRSS1)
NR_172949.1:n.384A>G (PRSS1)
NR_172950.1:n.298A>G (PRSS1)
NR_172951.1:n.232A>G (PRSS1)