Canonical Allele Identifier: CA1108082672

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753908_142753909del , CM000669.2:g.142753908_142753909del GRCh38
NC_000007.13:g.142461759_142461760del , CM000669.1:g.142461759_142461760del GRCh37
NC_000007.12:g.142141333_142141334del NCBI36
NG_008307.3:g.9425_9426del

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32722_370+32723del (TRBC1) ENSP00000482915.1:n.370+32722_370+32723del
ENST00000612126.4:c.591+1341_591+1342del (PRSS1) ENSP00000479959.1:n.591+1341_591+1342del
ENST00000633114.1:c.321+2014_321+2015del (PRSS2) ENSP00000487822.1:n.321+2014_321+2015del
ENST00000634019.1:c.82+5117_82+5118del (PRSS2) ENSP00000488594.1:n.82+5117_82+5118del