Canonical Allele Identifier: CA1108082283

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753660_142753663del , CM000669.2:g.142753660_142753663del GRCh38
NC_000007.13:g.142461511_142461514del , CM000669.1:g.142461511_142461514del GRCh37
NC_000007.12:g.142141085_142141088del NCBI36
NG_008307.3:g.9177_9180del

Transcript Alleles

HGVS Amino-acid change
ENST00000610416.2:c.370+32474_370+32477del (TRBC1) ENSP00000482915.1:n.370+32474_370+32477del
ENST00000612126.4:c.591+1093_591+1096del (PRSS1) ENSP00000479959.1:n.591+1093_591+1096del
ENST00000633114.1:c.321+1766_321+1769del (PRSS2) ENSP00000487822.1:n.321+1766_321+1769del
ENST00000634019.1:c.82+4869_82+4872del (PRSS2) ENSP00000488594.1:n.82+4869_82+4872del