Canonical Allele Identifier: CA2739299262

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142749824_142753738dup , CM000669.2:g.142749824_142753738dup GRCh38
NG_008307.3:g.5341_9255dup

Transcript Alleles

HGVS Amino-acid change
ENST00000610416.2:c.370+28638_370+32552dup (TRBC1) ENSP00000482915.1:n.370+28638_370+32552du...
ENST00000612126.4:c.40+300_591+1171dup (PRSS1)
ENST00000633114.1:c.40+300_321+1844dup (PRSS2)
ENST00000634019.1:c.82+1033_82+4947dup (PRSS2) ENSP00000488594.1:n.82+1033_82+4947dup