Canonical Allele Identifier: CA1139660291

Linked Data

ClinVar Variation Id: 973568
ClinVar RCV Id: RCV001250210

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142749126_142753040dup , CM000669.2:g.142749126_142753040dup GRCh38
NG_008307.3:g.4643_8557dup

Transcript Alleles

HGVS Amino-acid change
ENST00000610416.2:c.370+27940_370+31854dup (TRBC1) ENSP00000482915.1:n.370+27940_370+31854du...
ENST00000634019.1:c.82+335_82+4249dup (PRSS2) ENSP00000488594.1:n.82+335_82+4249dup
XM_011516411.1:c.427-110_*20dup (PRSS1)