Canonical Allele Identifier: CA168148978

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• dbSNP Id: rs188416614
• gnomAD v3: 7-142752177-A-G
• gnomAD v4: 7-142752177-A-G
• MyVariant Identifiers: chr7:g.142460028A>G (hg19) ; chr7:g.142752177A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752177A>G , CM000669.2:g.142752177A>G	GRCh38
NC_000007.13:g.142460028A>G , CM000669.1:g.142460028A>G	GRCh37
NC_000007.12:g.142139602A>G	NCBI36
NG_008307.3:g.7694A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.454+150A>G (PRSS1) MANE Select	ENSP00000308720.7:n.454+150A>G
ENST00000311737.11:c.454+150A>G (PRSS1)	ENSP00000308720.7:n.454+150A>G
ENST00000463701.1:n.918+150A>G (PRSS1)
ENST00000486171.5:c.496+150A>G (PRSS1)	ENSP00000417854.1:n.496+150A>G
ENST00000492062.1:c.304+150A>G (PRSS1)	ENSP00000419912.1:n.304+150A>G
ENST00000610416.2:c.370+30991A>G (TRBC1)	ENSP00000482915.1:n.370+30991A>G
ENST00000612126.4:c.454+150A>G (PRSS1)	ENSP00000479959.1:n.454+150A>G
ENST00000619214.4:c.424+150A>G (PRSS1)	ENSP00000481361.1:n.424+150A>G
ENST00000633114.1:c.321+283A>G (PRSS2)	ENSP00000487822.1:n.321+283A>G
ENST00000634019.1:c.82+3386A>G (PRSS2)	ENSP00000488594.1:n.82+3386A>G
NM_002769.4:c.454+150A>G (PRSS1)	NP_002760.1:n.454+150A>G
XM_011516411.1:c.1129+150A>G (PRSS1)	XP_011514713.1:n.1129+150A>G
NM_002769.5:c.454+150A>G (PRSS1) MANE Select	NP_002760.1:n.454+150A>G
NR_172947.1:n.396+150A>G (PRSS1)
NR_172948.1:n.393+150A>G (PRSS1)
NR_172949.1:n.393+150A>G (PRSS1)
NR_172950.1:n.307+150A>G (PRSS1)
NR_172951.1:n.241+150A>G (PRSS1)