Canonical Allele Identifier: CA168148974

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• dbSNP Id: rs905806047
• gnomAD v3: 7-142752155-C-T
• gnomAD v4: 7-142752155-C-T
• MyVariant Identifiers: chr7:g.142460006C>T (hg19) ; chr7:g.142752155C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752155C>T , CM000669.2:g.142752155C>T	GRCh38
NC_000007.13:g.142460006C>T , CM000669.1:g.142460006C>T	GRCh37
NC_000007.12:g.142139580C>T	NCBI36
NG_008307.3:g.7672C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.454+128C>T (PRSS1) MANE Select	ENSP00000308720.7:n.454+128C>T
ENST00000311737.11:c.454+128C>T (PRSS1)	ENSP00000308720.7:n.454+128C>T
ENST00000463701.1:n.918+128C>T (PRSS1)
ENST00000486171.5:c.496+128C>T (PRSS1)	ENSP00000417854.1:n.496+128C>T
ENST00000492062.1:c.304+128C>T (PRSS1)	ENSP00000419912.1:n.304+128C>T
ENST00000610416.2:c.370+30969C>T (TRBC1)	ENSP00000482915.1:n.370+30969C>T
ENST00000612126.4:c.454+128C>T (PRSS1)	ENSP00000479959.1:n.454+128C>T
ENST00000619214.4:c.424+128C>T (PRSS1)	ENSP00000481361.1:n.424+128C>T
ENST00000633114.1:c.321+261C>T (PRSS2)	ENSP00000487822.1:n.321+261C>T
ENST00000634019.1:c.82+3364C>T (PRSS2)	ENSP00000488594.1:n.82+3364C>T
NM_002769.4:c.454+128C>T (PRSS1)	NP_002760.1:n.454+128C>T
XM_011516411.1:c.1129+128C>T (PRSS1)	XP_011514713.1:n.1129+128C>T
NM_002769.5:c.454+128C>T (PRSS1) MANE Select	NP_002760.1:n.454+128C>T
NR_172947.1:n.396+128C>T (PRSS1)
NR_172948.1:n.393+128C>T (PRSS1)
NR_172949.1:n.393+128C>T (PRSS1)
NR_172950.1:n.307+128C>T (PRSS1)
NR_172951.1:n.241+128C>T (PRSS1)