Canonical Allele Identifier: CA260519
Gene: PRSS1 HGNC NCBI
TRBC1 HGNC NCBI
PRSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36705
ClinVar RCV Id: RCV000030384
dbSNP Id: rs193922656
MyVariant Identifiers: chr7:g.142459822C>G (hg19) chr7:g.142751971C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142751971C>G , CM000669.2:g.142751971C>G GRCh38
NC_000007.13:g.142459822C>G , CM000669.1:g.142459822C>G GRCh37
NC_000007.12:g.142139396C>G NCBI36
NG_008307.3:g.7488C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000311737.12:c.398C>G (PRSS1) MANE Select ENSP00000308720.7:p.Pro133Arg
ENST00000311737.11:c.398C>G (PRSS1) ENSP00000308720.7:p.Pro133Arg
ENST00000463701.1:n.862C>G (PRSS1)
ENST00000485223.1:n.1396C>G (PRSS1)
ENST00000486171.5:c.440C>G (PRSS1) ENSP00000417854.1:p.Pro147Arg
ENST00000492062.1:c.248C>G (PRSS1) ENSP00000419912.1:p.Pro83Arg
ENST00000610416.2:c.370+30785C>G (TRBC1) ENSP00000482915.1:n.370+30785C>G
ENST00000612126.4:c.398C>G (PRSS1) ENSP00000479959.1:p.Pro133Arg
ENST00000619214.4:c.368C>G (PRSS1) ENSP00000481361.1:p.Pro123Arg
ENST00000633114.1:c.321+77C>G (PRSS2) ENSP00000487822.1:n.321+77C>G
ENST00000634019.1:c.82+3180C>G (PRSS2) ENSP00000488594.1:n.82+3180C>G
NM_002769.4:c.398C>G (PRSS1) NP_002760.1:p.Pro133Arg
XM_011516411.1:c.1073C>G (PRSS1) XP_011514713.1:p.Pro358Arg
NM_002769.5:c.398C>G (PRSS1) MANE Select NP_002760.1:p.Pro133Arg
NR_172947.1:n.340C>G (PRSS1)
NR_172948.1:n.337C>G (PRSS1)
NR_172949.1:n.337C>G (PRSS1)
NR_172950.1:n.251C>G (PRSS1)
NR_172951.1:n.185C>G (PRSS1)
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