Canonical Allele Identifier: CA834446031

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• dbSNP Id: rs779079467
• gnomAD v4: 7-142753045-T-C
• MyVariant Identifiers: chr7:g.142460896T>C (hg19) ; chr7:g.142753045T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142753045T>C , CM000669.2:g.142753045T>C	GRCh38
NC_000007.13:g.142460896T>C , CM000669.1:g.142460896T>C	GRCh37
NC_000007.12:g.142140470T>C	NCBI36
NG_008307.3:g.8562T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000311737.12:c.*25T>C (PRSS1) MANE Select	ENSP00000308720.7:n.*25T>C
ENST00000311737.11:c.*25T>C (PRSS1)	ENSP00000308720.7:n.*25T>C
ENST00000463701.1:n.1233T>C (PRSS1)
ENST00000492062.1:c.602T>C (PRSS1)	ENSP00000419912.1:n.602T>C
ENST00000610416.2:c.370+31859T>C (TRBC1)	ENSP00000482915.1:n.370+31859T>C
ENST00000612126.4:c.591+478T>C (PRSS1)	ENSP00000479959.1:n.591+478T>C
ENST00000619214.4:c.*25T>C (PRSS1)	ENSP00000481361.1:n.*25T>C
ENST00000633114.1:c.321+1151T>C (PRSS2)	ENSP00000487822.1:n.321+1151T>C
ENST00000634019.1:c.82+4254T>C (PRSS2)	ENSP00000488594.1:n.82+4254T>C
NM_002769.4:c.*25T>C (PRSS1)	NP_002760.1:n.*25T>C
XM_011516411.1:c.*25T>C (PRSS1)	XP_011514713.1:n.*25T>C
NM_002769.5:c.*25T>C (PRSS1) MANE Select	NP_002760.1:n.*25T>C
NR_172947.1:n.711T>C (PRSS1)
NR_172948.1:n.708T>C (PRSS1)
NR_172949.1:n.708T>C (PRSS1)
NR_172950.1:n.622T>C (PRSS1)
NR_172951.1:n.556T>C (PRSS1)