Canonical Allele Identifier: CA1108082687

Linked Data

dbSNP Id: rs1798937016

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753915_142753918del , CM000669.2:g.142753915_142753918del GRCh38
NC_000007.13:g.142461766_142461769del , CM000669.1:g.142461766_142461769del GRCh37
NC_000007.12:g.142141340_142141343del NCBI36
NG_008307.3:g.9432_9435del

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32729_370+32732del (TRBC1) ENSP00000482915.1:n.370+32729_370+32732del
ENST00000612126.4:c.591+1348_591+1351del (PRSS1) ENSP00000479959.1:n.591+1348_591+1351del
ENST00000633114.1:c.321+2021_321+2024del (PRSS2) ENSP00000487822.1:n.321+2021_321+2024del
ENST00000634019.1:c.82+5124_82+5127del (PRSS2) ENSP00000488594.1:n.82+5124_82+5127del