Canonical Allele Identifier: CA1748625411

Linked Data

dbSNP Id: rs1798939404

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753957del , CM000669.2:g.142753957del GRCh38
NC_000007.13:g.142461808del , CM000669.1:g.142461808del GRCh37
NC_000007.12:g.142141382del NCBI36
NG_008307.3:g.9474del

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32771del (TRBC1) ENSP00000482915.1:n.370+32771del
ENST00000612126.4:c.591+1390del (PRSS1) ENSP00000479959.1:n.591+1390del
ENST00000633114.1:c.321+2063del (PRSS2) ENSP00000487822.1:n.321+2063del
ENST00000634019.1:c.82+5166del (PRSS2) ENSP00000488594.1:n.82+5166del