Canonical Allele Identifier: CA1748625287

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753770_142753771delinsCT , CM000669.2:g.142753770_142753771delinsCT GRCh38
NC_000007.13:g.142461621_142461622delinsCT , CM000669.1:g.142461621_142461622delinsCT GRCh37
NC_000007.12:g.142141195_142141196delinsCT NCBI36
NG_008307.3:g.9287_9288delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000610416.2:c.370+32584_370+32585delinsCT (TRBC1) ENSP00000482915.1:n.370+32584_370+32585delinsCT
ENST00000612126.4:c.591+1203_591+1204delinsCT (PRSS1) ENSP00000479959.1:n.591+1203_591+1204delinsCT
ENST00000633114.1:c.321+1876_321+1877delinsCT (PRSS2) ENSP00000487822.1:n.321+1876_321+1877delinsCT
ENST00000634019.1:c.82+4979_82+4980delinsCT (PRSS2) ENSP00000488594.1:n.82+4979_82+4980delinsCT