Canonical Allele Identifier: CA2685353277

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• gnomAD v4: 7-142753048-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142753048A>G , CM000669.2:g.142753048A>G	GRCh38
NC_000007.13:g.142460899A>G , CM000669.1:g.142460899A>G	GRCh37
NC_000007.12:g.142140473A>G	NCBI36
NG_008307.3:g.8565A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000311737.12:c.*28A>G (PRSS1) MANE Select	ENSP00000308720.7:n.*28A>G
ENST00000311737.11:c.*28A>G (PRSS1)	ENSP00000308720.7:n.*28A>G
ENST00000463701.1:n.1236A>G (PRSS1)
ENST00000492062.1:c.605A>G (PRSS1)	ENSP00000419912.1:n.605A>G
ENST00000610416.2:c.370+31862A>G (TRBC1)	ENSP00000482915.1:n.370+31862A>G
ENST00000612126.4:c.591+481A>G (PRSS1)	ENSP00000479959.1:n.591+481A>G
ENST00000619214.4:c.*28A>G (PRSS1)	ENSP00000481361.1:n.*28A>G
ENST00000633114.1:c.321+1154A>G (PRSS2)	ENSP00000487822.1:n.321+1154A>G
ENST00000634019.1:c.82+4257A>G (PRSS2)	ENSP00000488594.1:n.82+4257A>G
NM_002769.4:c.*28A>G (PRSS1)	NP_002760.1:n.*28A>G
XM_011516411.1:c.*28A>G (PRSS1)	XP_011514713.1:n.*28A>G
NM_002769.5:c.*28A>G (PRSS1) MANE Select	NP_002760.1:n.*28A>G
NR_172947.1:n.714A>G (PRSS1)
NR_172948.1:n.711A>G (PRSS1)
NR_172949.1:n.711A>G (PRSS1)
NR_172950.1:n.625A>G (PRSS1)
NR_172951.1:n.559A>G (PRSS1)