Canonical Allele Identifier: CA1748625285

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753767_142753768delinsCT , CM000669.2:g.142753767_142753768delinsCT GRCh38
NC_000007.13:g.142461618_142461619delinsCT , CM000669.1:g.142461618_142461619delinsCT GRCh37
NC_000007.12:g.142141192_142141193delinsCT NCBI36
NG_008307.3:g.9284_9285delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000610416.2:c.370+32581_370+32582delinsCT (TRBC1) ENSP00000482915.1:n.370+32581_370+32582delinsCT
ENST00000612126.4:c.591+1200_591+1201delinsCT (PRSS1) ENSP00000479959.1:n.591+1200_591+1201delinsCT
ENST00000633114.1:c.321+1873_321+1874delinsCT (PRSS2) ENSP00000487822.1:n.321+1873_321+1874delinsCT
ENST00000634019.1:c.82+4976_82+4977delinsCT (PRSS2) ENSP00000488594.1:n.82+4976_82+4977delinsCT