Canonical Allele Identifier: CA168152680

Linked Data

dbSNP Id: rs796256873

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753906_142753907delinsAA , CM000669.2:g.142753906_142753907delinsAA GRCh38
NC_000007.13:g.142461757_142461758delinsAA , CM000669.1:g.142461757_142461758delinsAA GRCh37
NC_000007.12:g.142141331_142141332delinsAA NCBI36
NG_008307.3:g.9423_9424delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32720_370+32721delinsAA (TRBC1) ENSP00000482915.1:n.370+32720_370+32721delinsAA
ENST00000612126.4:c.591+1339_591+1340delinsAA (PRSS1) ENSP00000479959.1:n.591+1339_591+1340delinsAA
ENST00000633114.1:c.321+2012_321+2013delinsAA (PRSS2) ENSP00000487822.1:n.321+2012_321+2013delinsAA
ENST00000634019.1:c.82+5115_82+5116delinsAA (PRSS2) ENSP00000488594.1:n.82+5115_82+5116delinsAA