Canonical Allele Identifier: CA369609268

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• gnomAD v3: 7-142752025-G-C
• gnomAD v4: 7-142752025-G-C
• MyVariant Identifiers: chr7:g.142459876G>C (hg19) ; chr7:g.142752025G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752025G>C , CM000669.2:g.142752025G>C	GRCh38
NC_000007.13:g.142459876G>C , CM000669.1:g.142459876G>C	GRCh37
NC_000007.12:g.142139450G>C	NCBI36
NG_008307.3:g.7542G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.452G>C (PRSS1) MANE Select	ENSP00000308720.7:p.Gly151Ala
ENST00000311737.11:c.452G>C (PRSS1)	ENSP00000308720.7:p.Gly151Ala
ENST00000463701.1:n.916G>C (PRSS1)
ENST00000486171.5:c.494G>C (PRSS1)	ENSP00000417854.1:p.Gly165Ala
ENST00000492062.1:c.302G>C (PRSS1)	ENSP00000419912.1:p.Gly101Ala
ENST00000610416.2:c.370+30839G>C (TRBC1)	ENSP00000482915.1:n.370+30839G>C
ENST00000612126.4:c.452G>C (PRSS1)	ENSP00000479959.1:p.Gly151Ala
ENST00000619214.4:c.422G>C (PRSS1)	ENSP00000481361.1:p.Gly141Ala
ENST00000633114.1:c.321+131G>C (PRSS2)	ENSP00000487822.1:n.321+131G>C
ENST00000634019.1:c.82+3234G>C (PRSS2)	ENSP00000488594.1:n.82+3234G>C
NM_002769.4:c.452G>C (PRSS1)	NP_002760.1:p.Gly151Ala
XM_011516411.1:c.1127G>C (PRSS1)	XP_011514713.1:p.Gly376Ala
NM_002769.5:c.452G>C (PRSS1) MANE Select	NP_002760.1:p.Gly151Ala
NR_172947.1:n.394G>C (PRSS1)
NR_172948.1:n.391G>C (PRSS1)
NR_172949.1:n.391G>C (PRSS1)
NR_172950.1:n.305G>C (PRSS1)
NR_172951.1:n.239G>C (PRSS1)